Canonical Allele Identifier: CA2615977069
Gene: DLAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025389T>A , CM000673.2:g.112025389T>A GRCh38
NC_000011.9:g.111896113T>A , CM000673.1:g.111896113T>A GRCh37
NC_000011.8:g.111401323T>A NCBI36
NG_013342.1:g.5576T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-84T>A ENSP00000518862.1:n.-84T>A
ENST00000280346.10:c.-84T>A ENSP00000280346.6:n.-84T>A
NM_001931.4:c.-84T>A NP_001922.2:n.-84T>A
XM_011542647.1:c.-84T>A XP_011540949.1:n.-84T>A
XM_011542647.3:c.-84T>A XP_011540949.1:n.-84T>A