Canonical Allele Identifier: CA388569250

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103508408A>T (hg19) ; chr13:g.102856058A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102856058A>T , CM000675.2:g.102856058A>T	GRCh38
NC_000013.10:g.103508408A>T , CM000675.1:g.103508408A>T	GRCh37
NC_000013.9:g.102306409A>T	NCBI36
NG_007146.1:g.15235A>T , LRG_464:g.15235A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.715A>T (ERCC5)
ENST00000682869.1:n.1123A>T (ERCC5)
ENST00000683246.1:n.1251A>T (ERCC5)
ENST00000684184.1:n.1120A>T (ERCC5)
ENST00000638434.1:c.572A>T (BIVM-ERCC5)
ENST00000639132.1:c.1149A>T (BIVM-ERCC5)	ENSP00000492684.1:p.Glu383Asp
ENST00000639435.1:c.1836A>T (BIVM-ERCC5)	ENSP00000491742.1:p.Glu612Asp
ENST00000651002.1:c.*235A>T (ERCC5)	ENSP00000498809.1:n.*235A>T
ENST00000651055.1:n.603A>T (ERCC5)
ENST00000651281.1:n.842A>T (ERCC5)
ENST00000651470.1:c.474A>T (ERCC5)	ENSP00000498701.1:p.Glu158Asp
ENST00000652225.2:c.474A>T (ERCC5) MANE Select	ENSP00000498881.2:p.Glu158Asp
ENST00000652613.1:c.-31A>T (ERCC5)	ENSP00000498357.1:n.-31A>T
ENST00000355739.8:c.474A>T (ERCC5)	ENSP00000347978.4:p.Glu158Asp
ENST00000535557.5:c.474A>T (ERCC5)	ENSP00000442117.1:p.Glu158Asp
ENST00000602836.1:c.1750A>T (BIVM-ERCC5)
ENST00000610537.4:c.474A>T (ERCC5)	ENSP00000478667.1:p.Glu158Asp
NM_000123.3:c.474A>T , LRG_464t1:c.474A>T (ERCC5)	NP_000114.2:p.Glu158Asp
NM_001204425.1:c.1836A>T (BIVM-ERCC5)	NP_001191354.1:p.Glu612Asp
NM_000123.4:c.474A>T (ERCC5) MANE Select	NP_000114.3:p.Glu158Asp
NM_001204425.2:c.1836A>T (BIVM-ERCC5)	NP_001191354.2:p.Glu612Asp