Canonical Allele Identifier: CA918969138

Gene: DLAT

Linked Data

• dbSNP Id: rs797036854

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025316_112025317delinsAG , CM000673.2:g.112025316_112025317delinsAG	GRCh38
NC_000011.9:g.111896040_111896041delinsAG , CM000673.1:g.111896040_111896041delinsAG	GRCh37
NC_000011.8:g.111401250_111401251delinsAG	NCBI36
NG_013342.1:g.5503_5504delinsAG

Transcript Alleles

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