Canonical Allele Identifier: CA2615977056
Gene: DLAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025374C>A , CM000673.2:g.112025374C>A GRCh38
NC_000011.9:g.111896098C>A , CM000673.1:g.111896098C>A GRCh37
NC_000011.8:g.111401308C>A NCBI36
NG_013342.1:g.5561C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-99C>A ENSP00000518862.1:n.-99C>A
ENST00000280346.10:c.-99C>A ENSP00000280346.6:n.-99C>A
NM_001931.4:c.-99C>A NP_001922.2:n.-99C>A
XM_011542647.1:c.-99C>A XP_011540949.1:n.-99C>A