Canonical Allele Identifier: CA2115203285
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102846025T= , CM000675.2:g.102846025T= GRCh38
NC_000013.10:g.103498375T= , CM000675.1:g.103498375T= GRCh37
NC_000013.9:g.102296376T= NCBI36
NG_007146.1:g.5202T= , LRG_464:g.5202T=

Transcript Alleles

HGVS Amino-acid change
ENST00000683246.1:n.121T= (ERCC5)
ENST00000638434.1:c.363-7732T= (BIVM-ERCC5)
ENST00000639118.1:c.363-3093T= (BIVM-ERCC5)
ENST00000639132.1:c.764-6093T= (BIVM-ERCC5) ENSP00000492684.1:n.764-6093T=
ENST00000639435.1:c.1451-6093T= (BIVM-ERCC5) ENSP00000491742.1:n.1451-6093T=
ENST00000651002.1:c.-242T= (ERCC5) ENSP00000498809.1:n.-242T=
ENST00000652613.1:c.-739T= (ERCC5) ENSP00000498357.1:n.-739T=
ENST00000355739.8:c.-242T= (ERCC5) ENSP00000347978.4:n.-242T=
ENST00000535557.5:c.-242T= (ERCC5) ENSP00000442117.1:n.-242T=
ENST00000602836.1:c.1365-6093T= (BIVM-ERCC5)
NM_000123.3:c.-242T= , LRG_464t1:c.-242T= (ERCC5) NP_000114.2:n.-242T=
NM_001204425.1:c.1451-6093T= (BIVM-ERCC5) NP_001191354.1:n.1451-6093T=
NM_001204425.2:c.1451-6093T= (BIVM-ERCC5) NP_001191354.2:n.1451-6093T=