Canonical Allele Identifier: CA2115208125
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1882419591

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102856310_102856311insGT , CM000675.2:g.102856310_102856311insGT GRCh38
NC_000013.10:g.103508660_103508661insGT , CM000675.1:g.103508660_103508661insGT GRCh37
NC_000013.9:g.102306661_102306662insGT NCBI36
NG_007146.1:g.15487_15488insGT , LRG_464:g.15487_15488insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.769+198_769+199insGT (ERCC5)
ENST00000682869.1:n.1177+198_1177+199insGT (ERCC5)
ENST00000683246.1:n.1305+198_1305+199insGT (ERCC5)
ENST00000684184.1:n.1174+198_1174+199insGT (ERCC5)
ENST00000639132.1:c.1203+198_1203+199insGT (BIVM-ERCC5) ENSP00000492684.1:n.1203+198_1203+199insGT
ENST00000639435.1:c.1890+198_1890+199insGT (BIVM-ERCC5) ENSP00000491742.1:n.1890+198_1890+199insGT
ENST00000651002.1:c.*289+198_*289+199insGT (ERCC5) ENSP00000498809.1:n.*289+198_*289+199insGT
ENST00000651055.1:n.657+198_657+199insGT (ERCC5)
ENST00000651281.1:n.896+198_896+199insGT (ERCC5)
ENST00000651470.1:c.528+198_528+199insGT (ERCC5) ENSP00000498701.1:n.528+198_528+199insGT
ENST00000652225.2:c.528+198_528+199insGT (ERCC5) MANE Select ENSP00000498881.2:n.528+198_528+199insGT
ENST00000652613.1:c.24+198_24+199insGT (ERCC5) ENSP00000498357.1:n.24+198_24+199insGT
ENST00000355739.8:c.528+198_528+199insGT (ERCC5) ENSP00000347978.4:n.528+198_528+199insGT
ENST00000535557.5:c.528+198_528+199insGT (ERCC5) ENSP00000442117.1:n.528+198_528+199insGT
ENST00000602836.1:c.1804+198_1804+199insGT (BIVM-ERCC5)
ENST00000610537.4:c.528+198_528+199insGT (ERCC5) ENSP00000478667.1:n.528+198_528+199insGT
NM_000123.3:c.528+198_528+199insGT , LRG_464t1:c.528+198_528+199insGT (ERCC5) NP_000114.2:n.528+198_528+199insGT
NM_001204425.1:c.1890+198_1890+199insGT (BIVM-ERCC5) NP_001191354.1:n.1890+198_1890+199insGT
NM_000123.4:c.528+198_528+199insGT (ERCC5) MANE Select NP_000114.3:n.528+198_528+199insGT
NM_001204425.2:c.1890+198_1890+199insGT (BIVM-ERCC5) NP_001191354.2:n.1890+198_1890+199insGT