Canonical Allele Identifier: CA2615977008

Gene: DLAT

Linked Data

• gnomAD v4: 11-112025321-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025321T>A , CM000673.2:g.112025321T>A	GRCh38
NC_000011.9:g.111896045T>A , CM000673.1:g.111896045T>A	GRCh37
NC_000011.8:g.111401255T>A	NCBI36
NG_013342.1:g.5508T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-152T>A	ENSP00000518862.1:n.-152T>A
ENST00000280346.10:c.-152T>A	ENSP00000280346.6:n.-152T>A
NM_001931.4:c.-152T>A	NP_001922.2:n.-152T>A