Canonical Allele Identifier: CA484859228
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.103525672A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873322A>G , CM000675.2:g.102873322A>G GRCh38
NC_000013.10:g.103525672A>G , CM000675.1:g.103525672A>G GRCh37
NC_000013.9:g.102323673A>G NCBI36
NG_007146.1:g.32499A>G , LRG_464:g.32499A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4044A>G (ERCC5)
ENST00000682869.1:n.3592A>G (ERCC5)
ENST00000683246.1:n.4580A>G (ERCC5)
ENST00000683642.1:n.3173A>G (ERCC5)
ENST00000639132.1:c.3618A>G (BIVM-ERCC5) ENSP00000492684.1:p.Leu1206=
ENST00000639435.1:c.4305A>G (BIVM-ERCC5) ENSP00000491742.1:p.Leu1435=
ENST00000651002.1:c.*2704A>G (ERCC5) ENSP00000498809.1:n.*2704A>G
ENST00000651055.1:n.3070A>G (ERCC5)
ENST00000651281.1:n.3311A>G (ERCC5)
ENST00000651387.1:n.2427A>G (ERCC5)
ENST00000651470.1:c.*115A>G (ERCC5) ENSP00000498701.1:n.*115A>G
ENST00000652225.2:c.2943A>G (ERCC5) MANE Select ENSP00000498881.2:p.Leu981=
ENST00000652613.1:c.2439A>G (ERCC5) ENSP00000498357.1:p.Leu813=
ENST00000355739.8:c.2943A>G (ERCC5) ENSP00000347978.4:p.Leu981=
ENST00000375954.1:c.642A>G (ERCC5) ENSP00000365121.1:p.Leu214=
ENST00000610537.4:c.2940A>G (ERCC5) ENSP00000478667.1:p.Leu980=
NM_000123.3:c.2943A>G , LRG_464t1:c.2943A>G (ERCC5) NP_000114.2:p.Leu981=
NM_001204425.1:c.4305A>G (BIVM-ERCC5) NP_001191354.1:p.Leu1435=
NM_000123.4:c.2943A>G (ERCC5) MANE Select NP_000114.3:p.Leu981=
NM_001204425.2:c.4305A>G (BIVM-ERCC5) NP_001191354.2:p.Leu1435=