Canonical Allele Identifier: CA388674980
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875596G>T , CM000675.2:g.102875596G>T GRCh38
NC_000013.10:g.103527946G>T , CM000675.1:g.103527946G>T GRCh37
NC_000013.9:g.102325947G>T NCBI36
NG_007146.1:g.34773G>T , LRG_464:g.34773G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4355G>T (ERCC5)
ENST00000682869.1:n.3903G>T (ERCC5)
ENST00000683246.1:n.4891G>T (ERCC5)
ENST00000683642.1:n.3484G>T (ERCC5)
ENST00000639132.1:c.3929G>T (BIVM-ERCC5) ENSP00000492684.1:p.Gly1310Val
ENST00000639435.1:c.4616G>T (BIVM-ERCC5) ENSP00000491742.1:p.Gly1539Val
ENST00000651002.1:c.*3015G>T (ERCC5) ENSP00000498809.1:n.*3015G>T
ENST00000651055.1:n.3381G>T (ERCC5)
ENST00000651281.1:n.3622G>T (ERCC5)
ENST00000651387.1:n.2738G>T (ERCC5)
ENST00000651470.1:c.*426G>T (ERCC5) ENSP00000498701.1:n.*426G>T
ENST00000652225.2:c.3254G>T (ERCC5) MANE Select ENSP00000498881.2:p.Gly1085Val
ENST00000652613.1:c.2750G>T (ERCC5) ENSP00000498357.1:p.Gly917Val
ENST00000355739.8:c.3254G>T (ERCC5) ENSP00000347978.4:p.Gly1085Val
ENST00000375954.1:c.953G>T (ERCC5) ENSP00000365121.1:p.Gly318Val
ENST00000472247.1:n.414G>T (ERCC5)
ENST00000610537.4:c.3251G>T (ERCC5) ENSP00000478667.1:p.Gly1084Val
NM_000123.3:c.3254G>T , LRG_464t1:c.3254G>T (ERCC5) NP_000114.2:p.Gly1085Val
NM_001204425.1:c.4616G>T (BIVM-ERCC5) NP_001191354.1:p.Gly1539Val
NM_000123.4:c.3254G>T (ERCC5) MANE Select NP_000114.3:p.Gly1085Val
NM_001204425.2:c.4616G>T (BIVM-ERCC5) NP_001191354.2:p.Gly1539Val