Canonical Allele Identifier: CA2623613285

Gene: ERCC5 BIVM-ERCC5

Linked Data

• gnomAD v4: 13-102845936-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102845936G>A , CM000675.2:g.102845936G>A	GRCh38
NC_000013.10:g.103498286G>A , CM000675.1:g.103498286G>A	GRCh37
NC_000013.9:g.102296287G>A	NCBI36
NG_007146.1:g.5113G>A , LRG_464:g.5113G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000683246.1:n.32G>A (ERCC5)
ENST00000638434.1:c.363-7821G>A (BIVM-ERCC5)
ENST00000639118.1:c.363-3182G>A (BIVM-ERCC5)
ENST00000639132.1:c.763+6133G>A (BIVM-ERCC5)	ENSP00000492684.1:n.763+6133G>A
ENST00000639435.1:c.1450+6133G>A (BIVM-ERCC5)	ENSP00000491742.1:n.1450+6133G>A
ENST00000651002.1:c.-331G>A (ERCC5)	ENSP00000498809.1:n.-331G>A
ENST00000652613.1:c.-828G>A (ERCC5)	ENSP00000498357.1:n.-828G>A
ENST00000355739.8:c.-331G>A (ERCC5)	ENSP00000347978.4:n.-331G>A
ENST00000535557.5:c.-331G>A (ERCC5)	ENSP00000442117.1:n.-331G>A
ENST00000602836.1:c.1364+6133G>A (BIVM-ERCC5)
NM_000123.3:c.-331G>A , LRG_464t1:c.-331G>A (ERCC5)	NP_000114.2:n.-331G>A
NM_001204425.1:c.1450+6133G>A (BIVM-ERCC5)	NP_001191354.1:n.1450+6133G>A
NM_001204425.2:c.1450+6133G>A (BIVM-ERCC5)	NP_001191354.2:n.1450+6133G>A