Canonical Allele Identifier: CA2000527649
Gene: DLAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025293C= , CM000673.2:g.112025293C= GRCh38
NC_000011.9:g.111896017C= , CM000673.1:g.111896017C= GRCh37
NC_000011.8:g.111401227C= NCBI36
NG_013342.1:g.5480C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-180C= ENSP00000518862.1:n.-180C=
ENST00000280346.10:c.-180C= ENSP00000280346.6:n.-180C=
NM_001931.4:c.-180C= NP_001922.2:n.-180C=