Canonical Allele Identifier: CA2000527704

Gene: DLAT

Linked Data

• dbSNP Id: rs1861927290
• gnomAD v3: 11-112025373-A-G
• gnomAD v4: 11-112025373-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025373A>G , CM000673.2:g.112025373A>G	GRCh38
NC_000011.9:g.111896097A>G , CM000673.1:g.111896097A>G	GRCh37
NC_000011.8:g.111401307A>G	NCBI36
NG_013342.1:g.5560A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-100A>G	ENSP00000518862.1:n.-100A>G
ENST00000280346.10:c.-100A>G	ENSP00000280346.6:n.-100A>G
NM_001931.4:c.-100A>G	NP_001922.2:n.-100A>G
XM_011542647.1:c.-100A>G	XP_011540949.1:n.-100A>G