Product Details

Assay Reference Genome
Location

Chr.11:47466656 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
Within Exon 21
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
CELF1 NM_001025596.2 13 3746 NP_001020767.1
NM_001172639.1 16 6706 NP_001166110.1
NM_001172640.1 13 6954 NP_001166111.1
NM_006560.3 14 3983 NP_006551.1
NM_198700.2 14 3928 NP_941989.1
XM_011519848.2 14 5485 XP_011518150.1
XM_011519850.2 14 7268 XP_011518152.2
XM_011519852.2 15 7468 XP_011518154.1
XM_011519854.1 17 7576 XP_011518156.1
XM_011519855.1 13 7297 XP_011518157.1
XM_011519856.1 14 7378 XP_011518158.1
XM_011519857.1 13 7249 XP_011518159.1
XM_011519858.1 13 7344 XP_011518160.1
XM_011519859.1 18 4265 XP_011518161.1
XM_017017101.1 16 7460 XP_016872590.1
XM_017017102.1 16 7291 XP_016872591.1
XM_017017103.1 15 5637 XP_016872592.1
XM_017017104.1 15 3973 XP_016872593.1
XM_017017105.1 15 7181 XP_016872594.1
XM_017017106.1 17 5822 XP_016872595.1
XM_017017107.1 15 3970 XP_016872596.1
XM_017017108.1 14 7260 XP_016872597.1
XM_017017109.1 14 7259 XP_016872598.1
XM_017017110.1 15 3961 XP_016872599.1
XM_017017111.1 14 7257 XP_016872600.1
XM_017017112.1 15 7169 XP_016872601.1
XM_017017113.1 15 5622 XP_016872602.1
XM_017017114.1 15 3958 XP_016872603.1
XM_017017115.1 15 7300 XP_016872604.1
XM_017017116.1 14 7335 XP_016872605.1
XM_017017117.1 13 7096 XP_016872606.1
XM_017017118.1 14 7130 XP_016872607.1
XM_017017119.1 16 7349 XP_016872608.1
XM_017017120.1 14 7161 XP_016872609.1
XM_017017121.1 14 7256 XP_016872610.1
XM_017017122.1 14 5614 XP_016872611.1
XM_017017123.1 14 3998 XP_016872612.1
XM_017017124.1 15 7388 XP_016872613.1
XM_017017125.1 13 7117 XP_016872614.1
XM_017017126.1 13 7246 XP_016872615.1
XM_017017127.1 13 7270 XP_016872616.1
XM_017017128.1 14 7206 XP_016872617.1
XM_017017129.1 15 7204 XP_016872618.1
XM_017017130.1 14 7158 XP_016872619.1
XM_017017131.1 14 7182 XP_016872620.1
XM_017017132.1 14 3995 XP_016872621.1
XM_017017133.1 13 7076 XP_016872622.1
XM_017017134.1 15 7127 XP_016872623.1
XM_017017135.1 13 7234 XP_016872624.1
AF248648.1 AAF86230.1
AK054655.1 1 2851
AK057016.1 1 1662

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 CELF1 PSMC3 MIR4487 MADD MYBPC3 SPI1 RAPSN SLC39A13

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