Canonical Allele Identifier: CA2615977026
Gene: DLAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025339G>A , CM000673.2:g.112025339G>A GRCh38
NC_000011.9:g.111896063G>A , CM000673.1:g.111896063G>A GRCh37
NC_000011.8:g.111401273G>A NCBI36
NG_013342.1:g.5526G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-134G>A ENSP00000518862.1:n.-134G>A
ENST00000280346.10:c.-134G>A ENSP00000280346.6:n.-134G>A
NM_001931.4:c.-134G>A NP_001922.2:n.-134G>A