Canonical Allele Identifier: CA2615977076
Gene: DLAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025398C>G , CM000673.2:g.112025398C>G GRCh38
NC_000011.9:g.111896122C>G , CM000673.1:g.111896122C>G GRCh37
NC_000011.8:g.111401332C>G NCBI36
NG_013342.1:g.5585C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-75C>G ENSP00000518862.1:n.-75C>G
ENST00000280346.10:c.-75C>G ENSP00000280346.6:n.-75C>G
NM_001931.4:c.-75C>G NP_001922.2:n.-75C>G
XM_011542647.1:c.-75C>G XP_011540949.1:n.-75C>G
XM_011542647.3:c.-75C>G XP_011540949.1:n.-75C>G