Canonical Allele Identifier: CA2000527679
Gene: DLAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025338G= , CM000673.2:g.112025338G= GRCh38
NC_000011.9:g.111896062G= , CM000673.1:g.111896062G= GRCh37
NC_000011.8:g.111401272G= NCBI36
NG_013342.1:g.5525G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-135G= ENSP00000518862.1:n.-135G=
ENST00000280346.10:c.-135G= ENSP00000280346.6:n.-135G=
NM_001931.4:c.-135G= NP_001922.2:n.-135G=