Canonical Allele Identifier: CA2000527671

Gene: DLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025316_112025317delinsGC , CM000673.2:g.112025316_112025317delinsGC	GRCh38
NC_000011.9:g.111896040_111896041delinsGC , CM000673.1:g.111896040_111896041delinsGC	GRCh37
NC_000011.8:g.111401250_111401251delinsGC	NCBI36
NG_013342.1:g.5503_5504delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-157_-156delinsGC	ENSP00000518862.1:n.-157_-156delinsGC
ENST00000280346.10:c.-157_-156delinsGC	ENSP00000280346.6:n.-157_-156delinsGC
NM_001931.4:c.-157_-156delinsGC	NP_001922.2:n.-157_-156delinsGC