Canonical Allele Identifier: CA255208098

Gene: ERCC5 BIVM-ERCC5

Linked Data

• dbSNP Id: rs111985238
• gnomAD v3: 13-102846105-T-A
• gnomAD v4: 13-102846105-T-A
• MyVariant Identifiers: chr13:g.103498455T>A (hg19) ; chr13:g.102846105T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102846105T>A , CM000675.2:g.102846105T>A	GRCh38
NC_000013.10:g.103498455T>A , CM000675.1:g.103498455T>A	GRCh37
NC_000013.9:g.102296456T>A	NCBI36
NG_007146.1:g.5282T>A , LRG_464:g.5282T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.80T>A (ERCC5)
ENST00000682869.1:n.73T>A (ERCC5)
ENST00000683246.1:n.201T>A (ERCC5)
ENST00000684184.1:n.70T>A (ERCC5)
ENST00000638434.1:c.363-7652T>A (BIVM-ERCC5)
ENST00000639118.1:c.363-3013T>A (BIVM-ERCC5)
ENST00000639132.1:c.764-6013T>A (BIVM-ERCC5)	ENSP00000492684.1:n.764-6013T>A
ENST00000639435.1:c.1451-6013T>A (BIVM-ERCC5)	ENSP00000491742.1:n.1451-6013T>A
ENST00000651002.1:c.-162T>A (ERCC5)	ENSP00000498809.1:n.-162T>A
ENST00000652225.2:c.-162T>A (ERCC5) MANE Select	ENSP00000498881.2:n.-162T>A
ENST00000652613.1:c.-659T>A (ERCC5)	ENSP00000498357.1:n.-659T>A
ENST00000355739.8:c.-162T>A (ERCC5)	ENSP00000347978.4:n.-162T>A
ENST00000472151.1:c.-162T>A (ERCC5)	ENSP00000436083.1:n.-162T>A
ENST00000535557.5:c.-162T>A (ERCC5)	ENSP00000442117.1:n.-162T>A
ENST00000602836.1:c.1365-6013T>A (BIVM-ERCC5)
NM_000123.3:c.-162T>A , LRG_464t1:c.-162T>A (ERCC5)	NP_000114.2:n.-162T>A
NM_001204425.1:c.1451-6013T>A (BIVM-ERCC5)	NP_001191354.1:n.1451-6013T>A
NM_000123.4:c.-162T>A (ERCC5) MANE Select	NP_000114.3:n.-162T>A
NM_001204425.2:c.1451-6013T>A (BIVM-ERCC5)	NP_001191354.2:n.1451-6013T>A