Canonical Allele Identifier: CA2115216489
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875600A= , CM000675.2:g.102875600A= GRCh38
NC_000013.10:g.103527950A= , CM000675.1:g.103527950A= GRCh37
NC_000013.9:g.102325951A= NCBI36
NG_007146.1:g.34777A= , LRG_464:g.34777A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4359A= (ERCC5)
ENST00000682869.1:n.3907A= (ERCC5)
ENST00000683246.1:n.4895A= (ERCC5)
ENST00000683642.1:n.3488A= (ERCC5)
ENST00000639132.1:c.3933A= (BIVM-ERCC5) ENSP00000492684.1:p.Gly1311=
ENST00000639435.1:c.4620A= (BIVM-ERCC5) ENSP00000491742.1:p.Gly1540=
ENST00000651002.1:c.*3019A= (ERCC5) ENSP00000498809.1:n.*3019A=
ENST00000651055.1:n.3385A= (ERCC5)
ENST00000651281.1:n.3626A= (ERCC5)
ENST00000651387.1:n.2742A= (ERCC5)
ENST00000651470.1:c.*430A= (ERCC5) ENSP00000498701.1:n.*430A=
ENST00000652225.2:c.3258A= (ERCC5) MANE Select ENSP00000498881.2:p.Gly1086=
ENST00000652613.1:c.2754A= (ERCC5) ENSP00000498357.1:p.Gly918=
ENST00000355739.8:c.3258A= (ERCC5) ENSP00000347978.4:p.Gly1086=
ENST00000375954.1:c.957A= (ERCC5) ENSP00000365121.1:p.Gly319=
ENST00000472247.1:n.418A= (ERCC5)
ENST00000610537.4:c.3255A= (ERCC5) ENSP00000478667.1:p.Gly1085=
NM_000123.3:c.3258A= , LRG_464t1:c.3258A= (ERCC5) NP_000114.2:p.Gly1086=
NM_001204425.1:c.4620A= (BIVM-ERCC5) NP_001191354.1:p.Gly1540=
NM_000123.4:c.3258A= (ERCC5) MANE Select NP_000114.3:p.Gly1086=
NM_001204425.2:c.4620A= (BIVM-ERCC5) NP_001191354.2:p.Gly1540=