Canonical Allele Identifier: CA484859206
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.103525637A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873287A>C , CM000675.2:g.102873287A>C GRCh38
NC_000013.10:g.103525637A>C , CM000675.1:g.103525637A>C GRCh37
NC_000013.9:g.102323638A>C NCBI36
NG_007146.1:g.32464A>C , LRG_464:g.32464A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4009A>C (ERCC5)
ENST00000682869.1:n.3557A>C (ERCC5)
ENST00000683246.1:n.4545A>C (ERCC5)
ENST00000683642.1:n.3138A>C (ERCC5)
ENST00000639132.1:c.3583A>C (BIVM-ERCC5) ENSP00000492684.1:p.Arg1195=
ENST00000639435.1:c.4270A>C (BIVM-ERCC5) ENSP00000491742.1:p.Arg1424=
ENST00000651002.1:c.*2669A>C (ERCC5) ENSP00000498809.1:n.*2669A>C
ENST00000651055.1:n.3035A>C (ERCC5)
ENST00000651281.1:n.3276A>C (ERCC5)
ENST00000651387.1:n.2392A>C (ERCC5)
ENST00000651470.1:c.*80A>C (ERCC5) ENSP00000498701.1:n.*80A>C
ENST00000652225.2:c.2908A>C (ERCC5) MANE Select ENSP00000498881.2:p.Arg970=
ENST00000652613.1:c.2404A>C (ERCC5) ENSP00000498357.1:p.Arg802=
ENST00000355739.8:c.2908A>C (ERCC5) ENSP00000347978.4:p.Arg970=
ENST00000375954.1:c.607A>C (ERCC5) ENSP00000365121.1:p.Arg203=
ENST00000610537.4:c.2905A>C (ERCC5) ENSP00000478667.1:p.Arg969=
NM_000123.3:c.2908A>C , LRG_464t1:c.2908A>C (ERCC5) NP_000114.2:p.Arg970=
NM_001204425.1:c.4270A>C (BIVM-ERCC5) NP_001191354.1:p.Arg1424=
NM_000123.4:c.2908A>C (ERCC5) MANE Select NP_000114.3:p.Arg970=
NM_001204425.2:c.4270A>C (BIVM-ERCC5) NP_001191354.2:p.Arg1424=