Canonical Allele Identifier: CA2000527661
Gene: DLAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025305G= , CM000673.2:g.112025305G= GRCh38
NC_000011.9:g.111896029G= , CM000673.1:g.111896029G= GRCh37
NC_000011.8:g.111401239G= NCBI36
NG_013342.1:g.5492G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-168G= ENSP00000518862.1:n.-168G=
ENST00000280346.10:c.-168G= ENSP00000280346.6:n.-168G=
NM_001931.4:c.-168G= NP_001922.2:n.-168G=