Canonical Allele Identifier: CA388569328

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103508438A>T (hg19) ; chr13:g.102856088A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102856088A>T , CM000675.2:g.102856088A>T	GRCh38
NC_000013.10:g.103508438A>T , CM000675.1:g.103508438A>T	GRCh37
NC_000013.9:g.102306439A>T	NCBI36
NG_007146.1:g.15265A>T , LRG_464:g.15265A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.745A>T (ERCC5)
ENST00000682869.1:n.1153A>T (ERCC5)
ENST00000683246.1:n.1281A>T (ERCC5)
ENST00000684184.1:n.1150A>T (ERCC5)
ENST00000638434.1:c.602A>T (BIVM-ERCC5)
ENST00000639132.1:c.1179A>T (BIVM-ERCC5)	ENSP00000492684.1:p.Arg393Ser
ENST00000639435.1:c.1866A>T (BIVM-ERCC5)	ENSP00000491742.1:p.Arg622Ser
ENST00000651002.1:c.*265A>T (ERCC5)	ENSP00000498809.1:n.*265A>T
ENST00000651055.1:n.633A>T (ERCC5)
ENST00000651281.1:n.872A>T (ERCC5)
ENST00000651470.1:c.504A>T (ERCC5)	ENSP00000498701.1:p.Arg168Ser
ENST00000652225.2:c.504A>T (ERCC5) MANE Select	ENSP00000498881.2:p.Arg168Ser
ENST00000652613.1:c.-1A>T (ERCC5)	ENSP00000498357.1:n.-1A>T
ENST00000355739.8:c.504A>T (ERCC5)	ENSP00000347978.4:p.Arg168Ser
ENST00000535557.5:c.504A>T (ERCC5)	ENSP00000442117.1:p.Arg168Ser
ENST00000602836.1:c.1780A>T (BIVM-ERCC5)
ENST00000610537.4:c.504A>T (ERCC5)	ENSP00000478667.1:p.Arg168Ser
NM_000123.3:c.504A>T , LRG_464t1:c.504A>T (ERCC5)	NP_000114.2:p.Arg168Ser
NM_001204425.1:c.1866A>T (BIVM-ERCC5)	NP_001191354.1:p.Arg622Ser
NM_000123.4:c.504A>T (ERCC5) MANE Select	NP_000114.3:p.Arg168Ser
NM_001204425.2:c.1866A>T (BIVM-ERCC5)	NP_001191354.2:p.Arg622Ser