Canonical Allele Identifier: CA2000527712
Gene: DLAT HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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