Canonical Allele Identifier: CA2623613288
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102845937G>T , CM000675.2:g.102845937G>T GRCh38
NC_000013.10:g.103498287G>T , CM000675.1:g.103498287G>T GRCh37
NC_000013.9:g.102296288G>T NCBI36
NG_007146.1:g.5114G>T , LRG_464:g.5114G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000683246.1:n.33G>T (ERCC5)
ENST00000638434.1:c.363-7820G>T (BIVM-ERCC5)
ENST00000639118.1:c.363-3181G>T (BIVM-ERCC5)
ENST00000639132.1:c.763+6134G>T (BIVM-ERCC5) ENSP00000492684.1:n.763+6134G>T
ENST00000639435.1:c.1450+6134G>T (BIVM-ERCC5) ENSP00000491742.1:n.1450+6134G>T
ENST00000651002.1:c.-330G>T (ERCC5) ENSP00000498809.1:n.-330G>T
ENST00000652613.1:c.-827G>T (ERCC5) ENSP00000498357.1:n.-827G>T
ENST00000355739.8:c.-330G>T (ERCC5) ENSP00000347978.4:n.-330G>T
ENST00000535557.5:c.-330G>T (ERCC5) ENSP00000442117.1:n.-330G>T
ENST00000602836.1:c.1364+6134G>T (BIVM-ERCC5)
NM_000123.3:c.-330G>T , LRG_464t1:c.-330G>T (ERCC5) NP_000114.2:n.-330G>T
NM_001204425.1:c.1450+6134G>T (BIVM-ERCC5) NP_001191354.1:n.1450+6134G>T
NM_001204425.2:c.1450+6134G>T (BIVM-ERCC5) NP_001191354.2:n.1450+6134G>T