Canonical Allele Identifier: CA2000527658

Gene: DLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025301_112025303delinsAAG , CM000673.2:g.112025301_112025303delinsAAG	GRCh38
NC_000011.9:g.111896025_111896027delinsAAG , CM000673.1:g.111896025_111896027delinsAAG	GRCh37
NC_000011.8:g.111401235_111401237delinsAAG	NCBI36
NG_013342.1:g.5488_5490delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-172_-170delinsAAG	ENSP00000518862.1:n.-172_-170delinsAAG
ENST00000280346.10:c.-172_-170delinsAAG	ENSP00000280346.6:n.-172_-170delinsAAG
NM_001931.4:c.-172_-170delinsAAG	NP_001922.2:n.-172_-170delinsAAG