Canonical Allele Identifier: CA2615977018

Gene: DLAT

Linked Data

• gnomAD v4: 11-112025330-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025334del , CM000673.2:g.112025334del	GRCh38
NC_000011.9:g.111896058del , CM000673.1:g.111896058del	GRCh37
NC_000011.8:g.111401268del	NCBI36
NG_013342.1:g.5521del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-139del	ENSP00000518862.1:n.-139del
ENST00000280346.10:c.-139del	ENSP00000280346.6:n.-139del
NM_001931.4:c.-139del	NP_001922.2:n.-139del