Canonical Allele Identifier: CA388673446
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873267A>G , CM000675.2:g.102873267A>G GRCh38
NC_000013.10:g.103525617A>G , CM000675.1:g.103525617A>G GRCh37
NC_000013.9:g.102323618A>G NCBI36
NG_007146.1:g.32444A>G , LRG_464:g.32444A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.3989A>G (ERCC5)
ENST00000682869.1:n.3537A>G (ERCC5)
ENST00000683246.1:n.4525A>G (ERCC5)
ENST00000683642.1:n.3118A>G (ERCC5)
ENST00000639132.1:c.3563A>G (BIVM-ERCC5) ENSP00000492684.1:p.Gln1188Arg
ENST00000639435.1:c.4250A>G (BIVM-ERCC5) ENSP00000491742.1:p.Gln1417Arg
ENST00000651002.1:c.*2649A>G (ERCC5) ENSP00000498809.1:n.*2649A>G
ENST00000651055.1:n.3015A>G (ERCC5)
ENST00000651281.1:n.3256A>G (ERCC5)
ENST00000651387.1:n.2372A>G (ERCC5)
ENST00000651470.1:c.*60A>G (ERCC5) ENSP00000498701.1:n.*60A>G
ENST00000652225.2:c.2888A>G (ERCC5) MANE Select ENSP00000498881.2:p.Gln963Arg
ENST00000652613.1:c.2384A>G (ERCC5) ENSP00000498357.1:p.Gln795Arg
ENST00000355739.8:c.2888A>G (ERCC5) ENSP00000347978.4:p.Gln963Arg
ENST00000375954.1:c.587A>G (ERCC5) ENSP00000365121.1:p.Gln196Arg
ENST00000610537.4:c.2885A>G (ERCC5) ENSP00000478667.1:p.Gln962Arg
NM_000123.3:c.2888A>G , LRG_464t1:c.2888A>G (ERCC5) NP_000114.2:p.Gln963Arg
NM_001204425.1:c.4250A>G (BIVM-ERCC5) NP_001191354.1:p.Gln1417Arg
NM_000123.4:c.2888A>G (ERCC5) MANE Select NP_000114.3:p.Gln963Arg
NM_001204425.2:c.4250A>G (BIVM-ERCC5) NP_001191354.2:p.Gln1417Arg