Canonical Allele Identifier: CA2574978774
Gene: DLAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025386C>T , CM000673.2:g.112025386C>T GRCh38
NC_000011.9:g.111896110C>T , CM000673.1:g.111896110C>T GRCh37
NC_000011.8:g.111401320C>T NCBI36
NG_013342.1:g.5573C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-87C>T ENSP00000518862.1:n.-87C>T
ENST00000280346.10:c.-87C>T ENSP00000280346.6:n.-87C>T
NM_001931.4:c.-87C>T NP_001922.2:n.-87C>T
XM_011542647.1:c.-87C>T XP_011540949.1:n.-87C>T
XM_011542647.3:c.-87C>T XP_011540949.1:n.-87C>T