Canonical Allele Identifier: CA484859207
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.103525639A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873289A>G , CM000675.2:g.102873289A>G GRCh38
NC_000013.10:g.103525639A>G , CM000675.1:g.103525639A>G GRCh37
NC_000013.9:g.102323640A>G NCBI36
NG_007146.1:g.32466A>G , LRG_464:g.32466A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4011A>G (ERCC5)
ENST00000682869.1:n.3559A>G (ERCC5)
ENST00000683246.1:n.4547A>G (ERCC5)
ENST00000683642.1:n.3140A>G (ERCC5)
ENST00000639132.1:c.3585A>G (BIVM-ERCC5) ENSP00000492684.1:p.Arg1195=
ENST00000639435.1:c.4272A>G (BIVM-ERCC5) ENSP00000491742.1:p.Arg1424=
ENST00000651002.1:c.*2671A>G (ERCC5) ENSP00000498809.1:n.*2671A>G
ENST00000651055.1:n.3037A>G (ERCC5)
ENST00000651281.1:n.3278A>G (ERCC5)
ENST00000651387.1:n.2394A>G (ERCC5)
ENST00000651470.1:c.*82A>G (ERCC5) ENSP00000498701.1:n.*82A>G
ENST00000652225.2:c.2910A>G (ERCC5) MANE Select ENSP00000498881.2:p.Arg970=
ENST00000652613.1:c.2406A>G (ERCC5) ENSP00000498357.1:p.Arg802=
ENST00000355739.8:c.2910A>G (ERCC5) ENSP00000347978.4:p.Arg970=
ENST00000375954.1:c.609A>G (ERCC5) ENSP00000365121.1:p.Arg203=
ENST00000610537.4:c.2907A>G (ERCC5) ENSP00000478667.1:p.Arg969=
NM_000123.3:c.2910A>G , LRG_464t1:c.2910A>G (ERCC5) NP_000114.2:p.Arg970=
NM_001204425.1:c.4272A>G (BIVM-ERCC5) NP_001191354.1:p.Arg1424=
NM_000123.4:c.2910A>G (ERCC5) MANE Select NP_000114.3:p.Arg970=
NM_001204425.2:c.4272A>G (BIVM-ERCC5) NP_001191354.2:p.Arg1424=