Canonical Allele Identifier: CA2115203367
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1881947780

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102846145G>A , CM000675.2:g.102846145G>A GRCh38
NC_000013.10:g.103498495G>A , CM000675.1:g.103498495G>A GRCh37
NC_000013.9:g.102296496G>A NCBI36
NG_007146.1:g.5322G>A , LRG_464:g.5322G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.120G>A (ERCC5)
ENST00000682869.1:n.113G>A (ERCC5)
ENST00000683246.1:n.241G>A (ERCC5)
ENST00000684184.1:n.110G>A (ERCC5)
ENST00000638434.1:c.363-7612G>A (BIVM-ERCC5)
ENST00000639118.1:c.363-2973G>A (BIVM-ERCC5)
ENST00000639132.1:c.764-5973G>A (BIVM-ERCC5) ENSP00000492684.1:n.764-5973G>A
ENST00000639435.1:c.1451-5973G>A (BIVM-ERCC5) ENSP00000491742.1:n.1451-5973G>A
ENST00000651002.1:c.-122G>A (ERCC5) ENSP00000498809.1:n.-122G>A
ENST00000652225.2:c.-122G>A (ERCC5) MANE Select ENSP00000498881.2:n.-122G>A
ENST00000652613.1:c.-619G>A (ERCC5) ENSP00000498357.1:n.-619G>A
ENST00000355739.8:c.-122G>A (ERCC5) ENSP00000347978.4:n.-122G>A
ENST00000375958.3:n.34G>A (ERCC5)
ENST00000472151.1:c.-122G>A (ERCC5) ENSP00000436083.1:n.-122G>A
ENST00000535557.5:c.-122G>A (ERCC5) ENSP00000442117.1:n.-122G>A
ENST00000602836.1:c.1365-5973G>A (BIVM-ERCC5)
NM_000123.3:c.-122G>A , LRG_464t1:c.-122G>A (ERCC5) NP_000114.2:n.-122G>A
NM_001204425.1:c.1451-5973G>A (BIVM-ERCC5) NP_001191354.1:n.1451-5973G>A
NM_000123.4:c.-122G>A (ERCC5) MANE Select NP_000114.3:n.-122G>A
NM_001204425.2:c.1451-5973G>A (BIVM-ERCC5) NP_001191354.2:n.1451-5973G>A