Canonical Allele Identifier: CA2615977087
Gene: DLAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025405G>A , CM000673.2:g.112025405G>A GRCh38
NC_000011.9:g.111896129G>A , CM000673.1:g.111896129G>A GRCh37
NC_000011.8:g.111401339G>A NCBI36
NG_013342.1:g.5592G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-68G>A ENSP00000518862.1:n.-68G>A
ENST00000280346.10:c.-68G>A ENSP00000280346.6:n.-68G>A
NM_001931.4:c.-68G>A NP_001922.2:n.-68G>A
XM_011542647.1:c.-68G>A XP_011540949.1:n.-68G>A
XM_011542647.3:c.-68G>A XP_011540949.1:n.-68G>A