Canonical Allele Identifier: CA388675018
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875616T>A , CM000675.2:g.102875616T>A GRCh38
NC_000013.10:g.103527966T>A , CM000675.1:g.103527966T>A GRCh37
NC_000013.9:g.102325967T>A NCBI36
NG_007146.1:g.34793T>A , LRG_464:g.34793T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4375T>A (ERCC5)
ENST00000682869.1:n.3923T>A (ERCC5)
ENST00000683246.1:n.4911T>A (ERCC5)
ENST00000683642.1:n.3504T>A (ERCC5)
ENST00000639132.1:c.3949T>A (BIVM-ERCC5) ENSP00000492684.1:p.Cys1317Ser
ENST00000639435.1:c.4636T>A (BIVM-ERCC5) ENSP00000491742.1:p.Cys1546Ser
ENST00000651002.1:c.*3035T>A (ERCC5) ENSP00000498809.1:n.*3035T>A
ENST00000651055.1:n.3401T>A (ERCC5)
ENST00000651281.1:n.3642T>A (ERCC5)
ENST00000651387.1:n.2758T>A (ERCC5)
ENST00000651470.1:c.*446T>A (ERCC5) ENSP00000498701.1:n.*446T>A
ENST00000652225.2:c.3274T>A (ERCC5) MANE Select ENSP00000498881.2:p.Cys1092Ser
ENST00000652613.1:c.2770T>A (ERCC5) ENSP00000498357.1:p.Cys924Ser
ENST00000355739.8:c.3274T>A (ERCC5) ENSP00000347978.4:p.Cys1092Ser
ENST00000375954.1:c.973T>A (ERCC5) ENSP00000365121.1:p.Cys325Ser
ENST00000472247.1:n.434T>A (ERCC5)
ENST00000610537.4:c.3271T>A (ERCC5) ENSP00000478667.1:p.Cys1091Ser
NM_000123.3:c.3274T>A , LRG_464t1:c.3274T>A (ERCC5) NP_000114.2:p.Cys1092Ser
NM_001204425.1:c.4636T>A (BIVM-ERCC5) NP_001191354.1:p.Cys1546Ser
NM_000123.4:c.3274T>A (ERCC5) MANE Select NP_000114.3:p.Cys1092Ser
NM_001204425.2:c.4636T>A (BIVM-ERCC5) NP_001191354.2:p.Cys1546Ser