Canonical Allele Identifier: CA2115208011
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102856079G= , CM000675.2:g.102856079G= GRCh38
NC_000013.10:g.103508429G= , CM000675.1:g.103508429G= GRCh37
NC_000013.9:g.102306430G= NCBI36
NG_007146.1:g.15256G= , LRG_464:g.15256G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.736G= (ERCC5)
ENST00000682869.1:n.1144G= (ERCC5)
ENST00000683246.1:n.1272G= (ERCC5)
ENST00000684184.1:n.1141G= (ERCC5)
ENST00000638434.1:c.593G= (BIVM-ERCC5)
ENST00000639132.1:c.1170G= (BIVM-ERCC5) ENSP00000492684.1:p.Trp390=
ENST00000639435.1:c.1857G= (BIVM-ERCC5) ENSP00000491742.1:p.Trp619=
ENST00000651002.1:c.*256G= (ERCC5) ENSP00000498809.1:n.*256G=
ENST00000651055.1:n.624G= (ERCC5)
ENST00000651281.1:n.863G= (ERCC5)
ENST00000651470.1:c.495G= (ERCC5) ENSP00000498701.1:p.Trp165=
ENST00000652225.2:c.495G= (ERCC5) MANE Select ENSP00000498881.2:p.Trp165=
ENST00000652613.1:c.-10G= (ERCC5) ENSP00000498357.1:n.-10G=
ENST00000355739.8:c.495G= (ERCC5) ENSP00000347978.4:p.Trp165=
ENST00000535557.5:c.495G= (ERCC5) ENSP00000442117.1:p.Trp165=
ENST00000602836.1:c.1771G= (BIVM-ERCC5)
ENST00000610537.4:c.495G= (ERCC5) ENSP00000478667.1:p.Trp165=
NM_000123.3:c.495G= , LRG_464t1:c.495G= (ERCC5) NP_000114.2:p.Trp165=
NM_001204425.1:c.1857G= (BIVM-ERCC5) NP_001191354.1:p.Trp619=
NM_000123.4:c.495G= (ERCC5) MANE Select NP_000114.3:p.Trp165=
NM_001204425.2:c.1857G= (BIVM-ERCC5) NP_001191354.2:p.Trp619=