Canonical Allele Identifier: CA942270718

Gene: DLAT

Linked Data

• dbSNP Id: rs1861926401
• gnomAD v3: 11-112025347-A-C
• gnomAD v4: 11-112025347-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025347A>C , CM000673.2:g.112025347A>C	GRCh38
NC_000011.9:g.111896071A>C , CM000673.1:g.111896071A>C	GRCh37
NC_000011.8:g.111401281A>C	NCBI36
NG_013342.1:g.5534A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-126A>C	ENSP00000518862.1:n.-126A>C
ENST00000280346.10:c.-126A>C	ENSP00000280346.6:n.-126A>C
NM_001931.4:c.-126A>C	NP_001922.2:n.-126A>C