Canonical Allele Identifier: CA2115203249
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1881939824
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102845976G>A , CM000675.2:g.102845976G>A GRCh38
NC_000013.10:g.103498326G>A , CM000675.1:g.103498326G>A GRCh37
NC_000013.9:g.102296327G>A NCBI36
NG_007146.1:g.5153G>A , LRG_464:g.5153G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000683246.1:n.72G>A (ERCC5)
ENST00000638434.1:c.363-7781G>A (BIVM-ERCC5)
ENST00000639118.1:c.363-3142G>A (BIVM-ERCC5)
ENST00000639132.1:c.764-6142G>A (BIVM-ERCC5) ENSP00000492684.1:n.764-6142G>A
ENST00000639435.1:c.1451-6142G>A (BIVM-ERCC5) ENSP00000491742.1:n.1451-6142G>A
ENST00000651002.1:c.-291G>A (ERCC5) ENSP00000498809.1:n.-291G>A
ENST00000652613.1:c.-788G>A (ERCC5) ENSP00000498357.1:n.-788G>A
ENST00000355739.8:c.-291G>A (ERCC5) ENSP00000347978.4:n.-291G>A
ENST00000535557.5:c.-291G>A (ERCC5) ENSP00000442117.1:n.-291G>A
ENST00000602836.1:c.1365-6142G>A (BIVM-ERCC5)
NM_000123.3:c.-291G>A , LRG_464t1:c.-291G>A (ERCC5) NP_000114.2:n.-291G>A
NM_001204425.1:c.1451-6142G>A (BIVM-ERCC5) NP_001191354.1:n.1451-6142G>A
NM_001204425.2:c.1451-6142G>A (BIVM-ERCC5) NP_001191354.2:n.1451-6142G>A
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