Canonical Allele Identifier: CA2000527653
Gene: DLAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025295T= , CM000673.2:g.112025295T= GRCh38
NC_000011.9:g.111896019T= , CM000673.1:g.111896019T= GRCh37
NC_000011.8:g.111401229T= NCBI36
NG_013342.1:g.5482T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-178T= ENSP00000518862.1:n.-178T=
ENST00000280346.10:c.-178T= ENSP00000280346.6:n.-178T=
NM_001931.4:c.-178T= NP_001922.2:n.-178T=