Canonical Allele Identifier: CA388675012

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103527962G>T (hg19) ; chr13:g.102875612G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102875612G>T , CM000675.2:g.102875612G>T	GRCh38
NC_000013.10:g.103527962G>T , CM000675.1:g.103527962G>T	GRCh37
NC_000013.9:g.102325963G>T	NCBI36
NG_007146.1:g.34789G>T , LRG_464:g.34789G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4371G>T (ERCC5)
ENST00000682869.1:n.3919G>T (ERCC5)
ENST00000683246.1:n.4907G>T (ERCC5)
ENST00000683642.1:n.3500G>T (ERCC5)
ENST00000639132.1:c.3945G>T (BIVM-ERCC5)	ENSP00000492684.1:p.Glu1315Asp
ENST00000639435.1:c.4632G>T (BIVM-ERCC5)	ENSP00000491742.1:p.Glu1544Asp
ENST00000651002.1:c.*3031G>T (ERCC5)	ENSP00000498809.1:n.*3031G>T
ENST00000651055.1:n.3397G>T (ERCC5)
ENST00000651281.1:n.3638G>T (ERCC5)
ENST00000651387.1:n.2754G>T (ERCC5)
ENST00000651470.1:c.*442G>T (ERCC5)	ENSP00000498701.1:n.*442G>T
ENST00000652225.2:c.3270G>T (ERCC5) MANE Select	ENSP00000498881.2:p.Glu1090Asp
ENST00000652613.1:c.2766G>T (ERCC5)	ENSP00000498357.1:p.Glu922Asp
ENST00000355739.8:c.3270G>T (ERCC5)	ENSP00000347978.4:p.Glu1090Asp
ENST00000375954.1:c.969G>T (ERCC5)	ENSP00000365121.1:p.Glu323Asp
ENST00000472247.1:n.430G>T (ERCC5)
ENST00000610537.4:c.3267G>T (ERCC5)	ENSP00000478667.1:p.Glu1089Asp
NM_000123.3:c.3270G>T , LRG_464t1:c.3270G>T (ERCC5)	NP_000114.2:p.Glu1090Asp
NM_001204425.1:c.4632G>T (BIVM-ERCC5)	NP_001191354.1:p.Glu1544Asp
NM_000123.4:c.3270G>T (ERCC5) MANE Select	NP_000114.3:p.Glu1090Asp
NM_001204425.2:c.4632G>T (BIVM-ERCC5)	NP_001191354.2:p.Glu1544Asp