Canonical Allele Identifier: CA484983672
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.103527971C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875621C>G , CM000675.2:g.102875621C>G GRCh38
NC_000013.10:g.103527971C>G , CM000675.1:g.103527971C>G GRCh37
NC_000013.9:g.102325972C>G NCBI36
NG_007146.1:g.34798C>G , LRG_464:g.34798C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4380C>G (ERCC5)
ENST00000682869.1:n.3928C>G (ERCC5)
ENST00000683246.1:n.4916C>G (ERCC5)
ENST00000683642.1:n.3509C>G (ERCC5)
ENST00000639132.1:c.3954C>G (BIVM-ERCC5) ENSP00000492684.1:p.Leu1318=
ENST00000639435.1:c.4641C>G (BIVM-ERCC5) ENSP00000491742.1:p.Leu1547=
ENST00000651002.1:c.*3040C>G (ERCC5) ENSP00000498809.1:n.*3040C>G
ENST00000651055.1:n.3406C>G (ERCC5)
ENST00000651281.1:n.3647C>G (ERCC5)
ENST00000651387.1:n.2763C>G (ERCC5)
ENST00000651470.1:c.*451C>G (ERCC5) ENSP00000498701.1:n.*451C>G
ENST00000652225.2:c.3279C>G (ERCC5) MANE Select ENSP00000498881.2:p.Leu1093=
ENST00000652613.1:c.2775C>G (ERCC5) ENSP00000498357.1:p.Leu925=
ENST00000355739.8:c.3279C>G (ERCC5) ENSP00000347978.4:p.Leu1093=
ENST00000375954.1:c.978C>G (ERCC5) ENSP00000365121.1:p.Leu326=
ENST00000472247.1:n.439C>G (ERCC5)
ENST00000610537.4:c.3276C>G (ERCC5) ENSP00000478667.1:p.Leu1092=
NM_000123.3:c.3279C>G , LRG_464t1:c.3279C>G (ERCC5) NP_000114.2:p.Leu1093=
NM_001204425.1:c.4641C>G (BIVM-ERCC5) NP_001191354.1:p.Leu1547=
NM_000123.4:c.3279C>G (ERCC5) MANE Select NP_000114.3:p.Leu1093=
NM_001204425.2:c.4641C>G (BIVM-ERCC5) NP_001191354.2:p.Leu1547=