Canonical Allele Identifier: CA942270738

Gene: DLAT

Linked Data

• dbSNP Id: rs1861927731
• gnomAD v3: 11-112025387-G-C
• gnomAD v4: 11-112025387-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112025387G>C , CM000673.2:g.112025387G>C	GRCh38
NC_000011.9:g.111896111G>C , CM000673.1:g.111896111G>C	GRCh37
NC_000011.8:g.111401321G>C	NCBI36
NG_013342.1:g.5574G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.-86G>C	ENSP00000518862.1:n.-86G>C
ENST00000280346.10:c.-86G>C	ENSP00000280346.6:n.-86G>C
NM_001931.4:c.-86G>C	NP_001922.2:n.-86G>C
XM_011542647.1:c.-86G>C	XP_011540949.1:n.-86G>C
XM_011542647.3:c.-86G>C	XP_011540949.1:n.-86G>C