Product Details

Assay Reference Genome
Location

Chr.11:47476857 on build GRCh38
Cytoband
11p11.2
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

Target Gene Details

Entrez Gene ID
10658
Gene Symbol
CELF1
Gene Name
CUGBP, Elav-like family member 1
Gene Aliases
BRUNOL2, CUG-BP, CUGBP, CUGBP1, EDEN-BP, NAB50, NAPOR, hNab50
Location
Chr.11:47465937-47565569 on build GRCh38
Assay Gene Location
Overlaps Intron 18 - Exon 18
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
CELF1 NM_001025596.2 NP_001020767.1
NM_001172639.1 NP_001166110.1
NM_001172640.1 NP_001166111.1
NM_006560.3 NP_006551.1
NM_198700.2 NP_941989.1
XM_011519848.2 XP_011518150.1
XM_011519850.2 XP_011518152.2
XM_011519852.2 XP_011518154.1
XM_011519854.1 XP_011518156.1
XM_011519855.1 XP_011518157.1
XM_011519856.1 XP_011518158.1
XM_011519857.1 XP_011518159.1
XM_011519858.1 XP_011518160.1
XM_011519859.1 XP_011518161.1
XM_017017101.1 XP_016872590.1
XM_017017102.1 XP_016872591.1
XM_017017103.1 XP_016872592.1
XM_017017104.1 XP_016872593.1
XM_017017105.1 XP_016872594.1
XM_017017106.1 XP_016872595.1
XM_017017107.1 XP_016872596.1
XM_017017108.1 XP_016872597.1
XM_017017109.1 XP_016872598.1
XM_017017110.1 XP_016872599.1
XM_017017111.1 XP_016872600.1
XM_017017112.1 XP_016872601.1
XM_017017113.1 XP_016872602.1
XM_017017114.1 XP_016872603.1
XM_017017115.1 XP_016872604.1
XM_017017116.1 XP_016872605.1
XM_017017117.1 XP_016872606.1
XM_017017118.1 XP_016872607.1
XM_017017119.1 XP_016872608.1
XM_017017120.1 XP_016872609.1
XM_017017121.1 XP_016872610.1
XM_017017122.1 XP_016872611.1
XM_017017123.1 XP_016872612.1
XM_017017124.1 XP_016872613.1
XM_017017125.1 XP_016872614.1
XM_017017126.1 XP_016872615.1
XM_017017127.1 XP_016872616.1
XM_017017128.1 XP_016872617.1
XM_017017129.1 XP_016872618.1
XM_017017130.1 XP_016872619.1
XM_017017131.1 XP_016872620.1
XM_017017132.1 XP_016872621.1
XM_017017133.1 XP_016872622.1
XM_017017134.1 XP_016872623.1
XM_017017135.1 XP_016872624.1
AB210019.1
AF248648.1 AAF86230.1
AF267533.1 AAF78955.1
AF267534.1 AAF78956.1
AJ007988.1 CAC20566.1
AK304430.1
AK307679.1
BC031079.1 AAH31079.1
U63289.1 AAC50895.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv832141 Chr11:47311629 - 47499441 on Build GRCh38 Loss MYBPC3 MADD SPI1 PSMC3 SLC39A13 RAPSN MIR4487 CELF1

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