Canonical Allele Identifier: CA2623613283
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102845935C>G , CM000675.2:g.102845935C>G GRCh38
NC_000013.10:g.103498285C>G , CM000675.1:g.103498285C>G GRCh37
NC_000013.9:g.102296286C>G NCBI36
NG_007146.1:g.5112C>G , LRG_464:g.5112C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000683246.1:n.31C>G (ERCC5)
ENST00000638434.1:c.363-7822C>G (BIVM-ERCC5)
ENST00000639118.1:c.363-3183C>G (BIVM-ERCC5)
ENST00000639132.1:c.763+6132C>G (BIVM-ERCC5) ENSP00000492684.1:n.763+6132C>G
ENST00000639435.1:c.1450+6132C>G (BIVM-ERCC5) ENSP00000491742.1:n.1450+6132C>G
ENST00000651002.1:c.-332C>G (ERCC5) ENSP00000498809.1:n.-332C>G
ENST00000652613.1:c.-829C>G (ERCC5) ENSP00000498357.1:n.-829C>G
ENST00000355739.8:c.-332C>G (ERCC5) ENSP00000347978.4:n.-332C>G
ENST00000535557.5:c.-332C>G (ERCC5) ENSP00000442117.1:n.-332C>G
ENST00000602836.1:c.1364+6132C>G (BIVM-ERCC5)
NM_000123.3:c.-332C>G , LRG_464t1:c.-332C>G (ERCC5) NP_000114.2:n.-332C>G
NM_001204425.1:c.1450+6132C>G (BIVM-ERCC5) NP_001191354.1:n.1450+6132C>G
NM_001204425.2:c.1450+6132C>G (BIVM-ERCC5) NP_001191354.2:n.1450+6132C>G