Canonical Allele Identifier: CA2623613614
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102846053T>C , CM000675.2:g.102846053T>C GRCh38
NC_000013.10:g.103498403T>C , CM000675.1:g.103498403T>C GRCh37
NC_000013.9:g.102296404T>C NCBI36
NG_007146.1:g.5230T>C , LRG_464:g.5230T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.28T>C (ERCC5)
ENST00000682869.1:n.21T>C (ERCC5)
ENST00000683246.1:n.149T>C (ERCC5)
ENST00000684184.1:n.18T>C (ERCC5)
ENST00000638434.1:c.363-7704T>C (BIVM-ERCC5)
ENST00000639118.1:c.363-3065T>C (BIVM-ERCC5)
ENST00000639132.1:c.764-6065T>C (BIVM-ERCC5) ENSP00000492684.1:n.764-6065T>C
ENST00000639435.1:c.1451-6065T>C (BIVM-ERCC5) ENSP00000491742.1:n.1451-6065T>C
ENST00000651002.1:c.-214T>C (ERCC5) ENSP00000498809.1:n.-214T>C
ENST00000652225.2:c.-214T>C (ERCC5) MANE Select ENSP00000498881.2:n.-214T>C
ENST00000652613.1:c.-711T>C (ERCC5) ENSP00000498357.1:n.-711T>C
ENST00000355739.8:c.-214T>C (ERCC5) ENSP00000347978.4:n.-214T>C
ENST00000472151.1:c.-214T>C (ERCC5) ENSP00000436083.1:n.-214T>C
ENST00000535557.5:c.-214T>C (ERCC5) ENSP00000442117.1:n.-214T>C
ENST00000602836.1:c.1365-6065T>C (BIVM-ERCC5)
NM_000123.3:c.-214T>C , LRG_464t1:c.-214T>C (ERCC5) NP_000114.2:n.-214T>C
NM_001204425.1:c.1451-6065T>C (BIVM-ERCC5) NP_001191354.1:n.1451-6065T>C
NM_000123.4:c.-214T>C (ERCC5) MANE Select NP_000114.3:n.-214T>C
NM_001204425.2:c.1451-6065T>C (BIVM-ERCC5) NP_001191354.2:n.1451-6065T>C