Canonical Allele Identifier: CA484983732
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.103527989A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875639A>C , CM000675.2:g.102875639A>C GRCh38
NC_000013.10:g.103527989A>C , CM000675.1:g.103527989A>C GRCh37
NC_000013.9:g.102325990A>C NCBI36
NG_007146.1:g.34816A>C , LRG_464:g.34816A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4398A>C (ERCC5)
ENST00000682869.1:n.3946A>C (ERCC5)
ENST00000683246.1:n.4934A>C (ERCC5)
ENST00000683642.1:n.3527A>C (ERCC5)
ENST00000639132.1:c.3972A>C (BIVM-ERCC5) ENSP00000492684.1:p.Gly1324=
ENST00000639435.1:c.4659A>C (BIVM-ERCC5) ENSP00000491742.1:p.Gly1553=
ENST00000651002.1:c.*3058A>C (ERCC5) ENSP00000498809.1:n.*3058A>C
ENST00000651055.1:n.3424A>C (ERCC5)
ENST00000651281.1:n.3665A>C (ERCC5)
ENST00000651387.1:n.2781A>C (ERCC5)
ENST00000651470.1:c.*469A>C (ERCC5) ENSP00000498701.1:n.*469A>C
ENST00000652225.2:c.3297A>C (ERCC5) MANE Select ENSP00000498881.2:p.Gly1099=
ENST00000652613.1:c.2793A>C (ERCC5) ENSP00000498357.1:p.Gly931=
ENST00000355739.8:c.3297A>C (ERCC5) ENSP00000347978.4:p.Gly1099=
ENST00000375954.1:c.996A>C (ERCC5) ENSP00000365121.1:p.Gly332=
ENST00000472247.1:n.457A>C (ERCC5)
ENST00000610537.4:c.3294A>C (ERCC5) ENSP00000478667.1:p.Gly1098=
NM_000123.3:c.3297A>C , LRG_464t1:c.3297A>C (ERCC5) NP_000114.2:p.Gly1099=
NM_001204425.1:c.4659A>C (BIVM-ERCC5) NP_001191354.1:p.Gly1553=
NM_000123.4:c.3297A>C (ERCC5) MANE Select NP_000114.3:p.Gly1099=
NM_001204425.2:c.4659A>C (BIVM-ERCC5) NP_001191354.2:p.Gly1553=