Canonical Allele Identifier: CA2623613280
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102845934C>T , CM000675.2:g.102845934C>T GRCh38
NC_000013.10:g.103498284C>T , CM000675.1:g.103498284C>T GRCh37
NC_000013.9:g.102296285C>T NCBI36
NG_007146.1:g.5111C>T , LRG_464:g.5111C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000683246.1:n.30C>T (ERCC5)
ENST00000638434.1:c.363-7823C>T (BIVM-ERCC5)
ENST00000639118.1:c.363-3184C>T (BIVM-ERCC5)
ENST00000639132.1:c.763+6131C>T (BIVM-ERCC5) ENSP00000492684.1:n.763+6131C>T
ENST00000639435.1:c.1450+6131C>T (BIVM-ERCC5) ENSP00000491742.1:n.1450+6131C>T
ENST00000651002.1:c.-333C>T (ERCC5) ENSP00000498809.1:n.-333C>T
ENST00000652613.1:c.-830C>T (ERCC5) ENSP00000498357.1:n.-830C>T
ENST00000355739.8:c.-333C>T (ERCC5) ENSP00000347978.4:n.-333C>T
ENST00000535557.5:c.-333C>T (ERCC5) ENSP00000442117.1:n.-333C>T
ENST00000602836.1:c.1364+6131C>T (BIVM-ERCC5)
NM_000123.3:c.-333C>T , LRG_464t1:c.-333C>T (ERCC5) NP_000114.2:n.-333C>T
NM_001204425.1:c.1450+6131C>T (BIVM-ERCC5) NP_001191354.1:n.1450+6131C>T
NM_001204425.2:c.1450+6131C>T (BIVM-ERCC5) NP_001191354.2:n.1450+6131C>T