Canonical Allele Identifier: CA1433035982
Gene: DGKQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.971014A= , CM000666.2:g.971014A= GRCh38
NC_000004.11:g.964802A= , CM000666.1:g.964802A= GRCh37
NC_000004.10:g.954802A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273814.8:c.330T= MANE Select ENSP00000273814.3:p.Ser110=
ENST00000273814.7:c.330T= ENSP00000273814.3:p.Ser110=
ENST00000509465.5:c.170T=
ENST00000510286.1:c.105T= ENSP00000427268.1:p.Ser35=
NM_001347.3:c.330T= NP_001338.2:p.Ser110=
XM_011513411.1:c.330T= XP_011511713.1:p.Ser110=
XM_011513412.1:c.330T= XP_011511714.1:p.Ser110=
XM_011513413.1:c.330T= XP_011511715.1:p.Ser110=
XM_011513414.1:c.330T= XP_011511716.1:p.Ser110=
XM_011513415.1:c.330T= XP_011511717.1:p.Ser110=
XM_011513414.2:c.330T= XP_011511716.1:p.Ser110=
XM_017007814.1:c.330T= XP_016863303.1:p.Ser110=
XM_017007815.1:c.330T= XP_016863304.1:p.Ser110=
XR_002959715.1:n.393T=
NM_001347.4:c.330T= MANE Select NP_001338.2:p.Ser110=