Canonical Allele Identifier: CA1433035971
Gene: DGKQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.971002G= , CM000666.2:g.971002G= GRCh38
NC_000004.11:g.964790G= , CM000666.1:g.964790G= GRCh37
NC_000004.10:g.954790G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273814.8:c.342C= MANE Select ENSP00000273814.3:p.Ser114=
ENST00000273814.7:c.342C= ENSP00000273814.3:p.Ser114=
ENST00000509465.5:c.182C=
ENST00000510286.1:c.117C= ENSP00000427268.1:p.Ser39=
NM_001347.3:c.342C= NP_001338.2:p.Ser114=
XM_011513411.1:c.342C= XP_011511713.1:p.Ser114=
XM_011513412.1:c.342C= XP_011511714.1:p.Ser114=
XM_011513413.1:c.342C= XP_011511715.1:p.Ser114=
XM_011513414.1:c.342C= XP_011511716.1:p.Ser114=
XM_011513415.1:c.342C= XP_011511717.1:p.Ser114=
XM_011513414.2:c.342C= XP_011511716.1:p.Ser114=
XM_017007814.1:c.342C= XP_016863303.1:p.Ser114=
XM_017007815.1:c.342C= XP_016863304.1:p.Ser114=
XR_002959715.1:n.405C=
NM_001347.4:c.342C= MANE Select NP_001338.2:p.Ser114=