Canonical Allele Identifier: CA1433036060
Gene: DGKQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.971061T= , CM000666.2:g.971061T= GRCh38
NC_000004.11:g.964849T= , CM000666.1:g.964849T= GRCh37
NC_000004.10:g.954849T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273814.8:c.283A= MANE Select ENSP00000273814.3:p.Met95=
ENST00000273814.7:c.283A= ENSP00000273814.3:p.Met95=
ENST00000509465.5:c.123A=
ENST00000510286.1:c.58A= ENSP00000427268.1:p.Met20=
NM_001347.3:c.283A= NP_001338.2:p.Met95=
XM_011513411.1:c.283A= XP_011511713.1:p.Met95=
XM_011513412.1:c.283A= XP_011511714.1:p.Met95=
XM_011513413.1:c.283A= XP_011511715.1:p.Met95=
XM_011513414.1:c.283A= XP_011511716.1:p.Met95=
XM_011513415.1:c.283A= XP_011511717.1:p.Met95=
XM_011513414.2:c.283A= XP_011511716.1:p.Met95=
XM_017007814.1:c.283A= XP_016863303.1:p.Met95=
XM_017007815.1:c.283A= XP_016863304.1:p.Met95=
XR_002959715.1:n.346A=
NM_001347.4:c.283A= MANE Select NP_001338.2:p.Met95=