Canonical Allele Identifier: CA2615977011

Gene: DLAT

Linked Data

• gnomAD v4: 11-112025325-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025327del , CM000673.2:g.112025327del	GRCh38
NC_000011.9:g.111896051del , CM000673.1:g.111896051del	GRCh37
NC_000011.8:g.111401261del	NCBI36
NG_013342.1:g.5514del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-146del	ENSP00000518862.1:n.-146del
ENST00000280346.10:c.-146del	ENSP00000280346.6:n.-146del
NM_001931.4:c.-146del	NP_001922.2:n.-146del