Canonical Allele Identifier: CA2623613861
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102846130G>T , CM000675.2:g.102846130G>T GRCh38
NC_000013.10:g.103498480G>T , CM000675.1:g.103498480G>T GRCh37
NC_000013.9:g.102296481G>T NCBI36
NG_007146.1:g.5307G>T , LRG_464:g.5307G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.105G>T (ERCC5)
ENST00000682869.1:n.98G>T (ERCC5)
ENST00000683246.1:n.226G>T (ERCC5)
ENST00000684184.1:n.95G>T (ERCC5)
ENST00000638434.1:c.363-7627G>T (BIVM-ERCC5)
ENST00000639118.1:c.363-2988G>T (BIVM-ERCC5)
ENST00000639132.1:c.764-5988G>T (BIVM-ERCC5) ENSP00000492684.1:n.764-5988G>T
ENST00000639435.1:c.1451-5988G>T (BIVM-ERCC5) ENSP00000491742.1:n.1451-5988G>T
ENST00000651002.1:c.-137G>T (ERCC5) ENSP00000498809.1:n.-137G>T
ENST00000652225.2:c.-137G>T (ERCC5) MANE Select ENSP00000498881.2:n.-137G>T
ENST00000652613.1:c.-634G>T (ERCC5) ENSP00000498357.1:n.-634G>T
ENST00000355739.8:c.-137G>T (ERCC5) ENSP00000347978.4:n.-137G>T
ENST00000375958.3:n.19G>T (ERCC5)
ENST00000472151.1:c.-137G>T (ERCC5) ENSP00000436083.1:n.-137G>T
ENST00000535557.5:c.-137G>T (ERCC5) ENSP00000442117.1:n.-137G>T
ENST00000602836.1:c.1365-5988G>T (BIVM-ERCC5)
NM_000123.3:c.-137G>T , LRG_464t1:c.-137G>T (ERCC5) NP_000114.2:n.-137G>T
NM_001204425.1:c.1451-5988G>T (BIVM-ERCC5) NP_001191354.1:n.1451-5988G>T
NM_000123.4:c.-137G>T (ERCC5) MANE Select NP_000114.3:n.-137G>T
NM_001204425.2:c.1451-5988G>T (BIVM-ERCC5) NP_001191354.2:n.1451-5988G>T