Canonical Allele Identifier: CA388574117
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102862877A>T , CM000675.2:g.102862877A>T GRCh38
NC_000013.10:g.103515227A>T , CM000675.1:g.103515227A>T GRCh37
NC_000013.9:g.102313228A>T NCBI36
NG_007146.1:g.22054A>T , LRG_464:g.22054A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.1969A>T (ERCC5)
ENST00000682869.1:n.2377A>T (ERCC5)
ENST00000683246.1:n.2505A>T (ERCC5)
ENST00000639132.1:c.2403A>T (BIVM-ERCC5) ENSP00000492684.1:p.Glu801Asp
ENST00000639435.1:c.3090A>T (BIVM-ERCC5) ENSP00000491742.1:p.Glu1030Asp
ENST00000651002.1:c.*1489A>T (ERCC5) ENSP00000498809.1:n.*1489A>T
ENST00000651055.1:n.1857A>T (ERCC5)
ENST00000651281.1:n.2096A>T (ERCC5)
ENST00000651387.1:n.1212A>T (ERCC5)
ENST00000651470.1:c.1728A>T (ERCC5) ENSP00000498701.1:p.Glu576Asp
ENST00000652225.2:c.1728A>T (ERCC5) MANE Select ENSP00000498881.2:p.Glu576Asp
ENST00000652613.1:c.1224A>T (ERCC5) ENSP00000498357.1:p.Glu408Asp
ENST00000355739.8:c.1728A>T (ERCC5) ENSP00000347978.4:p.Glu576Asp
ENST00000602836.1:c.3004A>T (BIVM-ERCC5)
ENST00000610537.4:c.1728A>T (ERCC5) ENSP00000478667.1:p.Glu576Asp
NM_000123.3:c.1728A>T , LRG_464t1:c.1728A>T (ERCC5) NP_000114.2:p.Glu576Asp
NM_001204425.1:c.3090A>T (BIVM-ERCC5) NP_001191354.1:p.Glu1030Asp
NM_000123.4:c.1728A>T (ERCC5) MANE Select NP_000114.3:p.Glu576Asp
NM_001204425.2:c.3090A>T (BIVM-ERCC5) NP_001191354.2:p.Glu1030Asp