Canonical Allele Identifier: CA2623613837
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102846126C>T , CM000675.2:g.102846126C>T GRCh38
NC_000013.10:g.103498476C>T , CM000675.1:g.103498476C>T GRCh37
NC_000013.9:g.102296477C>T NCBI36
NG_007146.1:g.5303C>T , LRG_464:g.5303C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.101C>T (ERCC5)
ENST00000682869.1:n.94C>T (ERCC5)
ENST00000683246.1:n.222C>T (ERCC5)
ENST00000684184.1:n.91C>T (ERCC5)
ENST00000638434.1:c.363-7631C>T (BIVM-ERCC5)
ENST00000639118.1:c.363-2992C>T (BIVM-ERCC5)
ENST00000639132.1:c.764-5992C>T (BIVM-ERCC5) ENSP00000492684.1:n.764-5992C>T
ENST00000639435.1:c.1451-5992C>T (BIVM-ERCC5) ENSP00000491742.1:n.1451-5992C>T
ENST00000651002.1:c.-141C>T (ERCC5) ENSP00000498809.1:n.-141C>T
ENST00000652225.2:c.-141C>T (ERCC5) MANE Select ENSP00000498881.2:n.-141C>T
ENST00000652613.1:c.-638C>T (ERCC5) ENSP00000498357.1:n.-638C>T
ENST00000355739.8:c.-141C>T (ERCC5) ENSP00000347978.4:n.-141C>T
ENST00000375958.3:n.15C>T (ERCC5)
ENST00000472151.1:c.-141C>T (ERCC5) ENSP00000436083.1:n.-141C>T
ENST00000535557.5:c.-141C>T (ERCC5) ENSP00000442117.1:n.-141C>T
ENST00000602836.1:c.1365-5992C>T (BIVM-ERCC5)
NM_000123.3:c.-141C>T , LRG_464t1:c.-141C>T (ERCC5) NP_000114.2:n.-141C>T
NM_001204425.1:c.1451-5992C>T (BIVM-ERCC5) NP_001191354.1:n.1451-5992C>T
NM_000123.4:c.-141C>T (ERCC5) MANE Select NP_000114.3:n.-141C>T
NM_001204425.2:c.1451-5992C>T (BIVM-ERCC5) NP_001191354.2:n.1451-5992C>T