Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGGACTTGGCGCCACAGGCTTGAC[A/G]AATGGCACGGCTGGCACCATGGACG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602538 | ||||||||||||||||||||
Literature Links: |
CELF2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CELF2 - CUGBP, Elav-like family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001025076.2 | 1445 | Silent Mutation | ACA,ACG | T,T 355 | NP_001020247.1 | |
NM_001025077.2 | 1445 | Silent Mutation | ACA,ACG | T,T 373 | NP_001020248.1 | |
NM_001083591.1 | 1445 | Silent Mutation | ACA,ACG | T,T 353 | NP_001077060.1 | |
NM_001326317.1 | 1445 | Silent Mutation | ACA,ACG | T,T 349 | NP_001313246.1 | |
NM_001326318.1 | 1445 | Silent Mutation | ACA,ACG | T,T 355 | NP_001313247.1 | |
NM_001326319.1 | 1445 | Silent Mutation | ACA,ACG | T,T 373 | NP_001313248.1 | |
NM_001326320.1 | 1445 | Silent Mutation | ACA,ACG | T,T 355 | NP_001313249.1 | |
NM_001326321.1 | 1445 | Silent Mutation | ACA,ACG | T,T 363 | NP_001313250.1 | |
NM_001326323.1 | 1445 | Silent Mutation | ACA,ACG | T,T 369 | NP_001313252.1 | |
NM_001326324.1 | 1445 | Silent Mutation | ACA,ACG | T,T 355 | NP_001313253.1 | |
NM_001326325.1 | 1445 | Silent Mutation | ACA,ACG | T,T 404 | NP_001313254.1 | |
NM_001326326.1 | 1445 | Silent Mutation | ACA,ACG | T,T 385 | NP_001313255.1 | |
NM_001326327.1 | 1445 | Silent Mutation | ACA,ACG | T,T 391 | NP_001313256.1 | |
NM_001326328.1 | 1445 | Silent Mutation | ACA,ACG | T,T 355 | NP_001313257.1 | |
NM_001326329.1 | 1445 | Silent Mutation | ACA,ACG | T,T 349 | NP_001313258.1 | |
NM_001326330.1 | 1445 | Silent Mutation | ACA,ACG | T,T 355 | NP_001313259.1 | |
NM_001326331.1 | 1445 | Silent Mutation | ACA,ACG | T,T 379 | NP_001313260.1 | |
NM_001326332.1 | 1445 | Silent Mutation | ACA,ACG | T,T 373 | NP_001313261.1 | |
NM_001326333.1 | 1445 | Silent Mutation | ACA,ACG | T,T 151 | NP_001313262.1 | |
NM_001326334.1 | 1445 | Silent Mutation | ACA,ACG | T,T 355 | NP_001313263.1 | |
NM_001326335.1 | 1445 | Silent Mutation | ACA,ACG | T,T 377 | NP_001313264.1 | |
NM_001326336.1 | 1445 | Silent Mutation | ACA,ACG | T,T 397 | NP_001313265.1 | |
NM_001326337.1 | 1445 | Intron | NP_001313266.1 | |||
NM_001326338.1 | 1445 | Silent Mutation | ACA,ACG | T,T 262 | NP_001313267.1 | |
NM_001326339.1 | 1445 | Silent Mutation | ACA,ACG | T,T 268 | NP_001313268.1 | |
NM_001326340.1 | 1445 | Silent Mutation | ACA,ACG | T,T 398 | NP_001313269.1 | |
NM_001326341.1 | 1445 | Silent Mutation | ACA,ACG | T,T 380 | NP_001313270.1 | |
NM_001326342.1 | 1445 | Silent Mutation | ACA,ACG | T,T 386 | NP_001313271.1 | |
NM_001326343.1 | 1445 | Silent Mutation | ACA,ACG | T,T 404 | NP_001313272.1 | |
NM_001326344.1 | 1445 | Silent Mutation | ACA,ACG | T,T 349 | NP_001313273.1 | |
NM_001326345.1 | 1445 | Silent Mutation | ACA,ACG | T,T 355 | NP_001313274.1 | |
NM_001326346.1 | 1445 | Silent Mutation | ACA,ACG | T,T 145 | NP_001313275.1 | |
NM_001326347.1 | 1445 | Silent Mutation | ACA,ACG | T,T 361 | NP_001313276.1 | |
NM_001326348.1 | 1445 | Silent Mutation | ACA,ACG | T,T 349 | NP_001313277.1 | |
NM_001326349.1 | 1445 | Silent Mutation | ACA,ACG | T,T 355 | NP_001313278.1 | |
NM_006561.3 | 1445 | Silent Mutation | ACA,ACG | T,T 386 | NP_006552.3 | |
XM_005252354.4 | 1445 | Silent Mutation | ACA,ACG | T,T 379 | XP_005252411.1 | |
XM_005252357.4 | 1445 | Silent Mutation | ACA,ACG | T,T 145 | XP_005252414.1 | |
XM_005252358.3 | 1445 | Silent Mutation | ACA,ACG | T,T 145 | XP_005252415.1 | |
XM_006717373.2 | 1445 | Silent Mutation | ACA,ACG | T,T 268 | XP_006717436.1 | |
XM_011519294.2 | 1445 | Silent Mutation | ACA,ACG | T,T 373 | XP_011517596.1 | |
XM_011519297.1 | 1445 | Silent Mutation | ACA,ACG | T,T 349 | XP_011517599.1 | |
XM_017015542.1 | 1445 | Silent Mutation | ACA,ACG | T,T 359 | XP_016871031.1 | |
XM_017015543.1 | 1445 | Silent Mutation | ACA,ACG | T,T 390 | XP_016871032.1 | |
XM_017015544.1 | 1445 | Silent Mutation | ACA,ACG | T,T 386 | XP_016871033.1 | |
XM_017015545.1 | 1445 | Silent Mutation | ACA,ACG | T,T 384 | XP_016871034.1 | |
XM_017015546.1 | 1445 | Silent Mutation | ACA,ACG | T,T 384 | XP_016871035.1 | |
XM_017015547.1 | 1445 | Silent Mutation | ACA,ACG | T,T 383 | XP_016871036.1 | |
XM_017015548.1 | 1445 | Silent Mutation | ACA,ACG | T,T 380 | XP_016871037.1 | |
XM_017015549.1 | 1445 | Silent Mutation | ACA,ACG | T,T 380 | XP_016871038.1 | |
XM_017015550.1 | 1445 | Silent Mutation | ACA,ACG | T,T 379 | XP_016871039.1 | |
XM_017015551.1 | 1445 | Silent Mutation | ACA,ACG | T,T 377 | XP_016871040.1 | |
XM_017015552.1 | 1445 | Silent Mutation | ACA,ACG | T,T 359 | XP_016871041.1 | |
XM_017015553.1 | 1445 | Silent Mutation | ACA,ACG | T,T 355 | XP_016871042.1 | |
XM_017015554.1 | 1445 | Silent Mutation | ACA,ACG | T,T 349 | XP_016871043.1 | |
XM_017015555.1 | 1445 | Intron | XP_016871044.1 | |||
XM_017015556.1 | 1445 | Silent Mutation | ACA,ACG | T,T 272 | XP_016871045.1 | |
XM_017015557.1 | 1445 | Silent Mutation | ACA,ACG | T,T 272 | XP_016871046.1 | |
XM_017015558.1 | 1445 | Silent Mutation | ACA,ACG | T,T 272 | XP_016871047.1 | |
XM_017015559.1 | 1445 | Silent Mutation | ACA,ACG | T,T 268 | XP_016871048.1 | |
XM_017015560.1 | 1445 | Silent Mutation | ACA,ACG | T,T 268 | XP_016871049.1 | |
XM_017015561.1 | 1445 | Silent Mutation | ACA,ACG | T,T 268 | XP_016871050.1 | |
XM_017015562.1 | 1445 | Silent Mutation | ACA,ACG | T,T 262 | XP_016871051.1 | |
XM_017015563.1 | 1445 | Silent Mutation | ACA,ACG | T,T 262 | XP_016871052.1 | |
XM_017015564.1 | 1445 | Silent Mutation | ACA,ACG | T,T 155 | XP_016871053.1 | |
XM_017015565.1 | 1445 | Silent Mutation | ACA,ACG | T,T 155 | XP_016871054.1 | |
XM_017015566.1 | 1445 | Silent Mutation | ACA,ACG | T,T 151 | XP_016871055.1 | |
XM_017015567.1 | 1445 | Silent Mutation | ACA,ACG | T,T 151 | XP_016871056.1 | |
XM_017015568.1 | 1445 | Silent Mutation | ACA,ACG | T,T 151 | XP_016871057.1 | |
XM_017015569.1 | 1445 | Silent Mutation | ACA,ACG | T,T 149 | XP_016871058.1 | |
XM_017015570.1 | 1445 | Silent Mutation | ACA,ACG | T,T 149 | XP_016871059.1 | |
XM_017015571.1 | 1445 | Silent Mutation | ACA,ACG | T,T 145 | XP_016871060.1 | |
XM_017015572.1 | 1445 | Silent Mutation | ACA,ACG | T,T 145 | XP_016871061.1 |
CELF2-AS1 - CELF2 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |