Canonical Allele Identifier: CA355941749
Gene: DGKQ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.971066T>G , CM000666.2:g.971066T>G GRCh38
NC_000004.11:g.964854T>G , CM000666.1:g.964854T>G GRCh37
NC_000004.10:g.954854T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273814.8:c.278A>C MANE Select ENSP00000273814.3:p.Asn93Thr
ENST00000273814.7:c.278A>C ENSP00000273814.3:p.Asn93Thr
ENST00000509465.5:c.118A>C
ENST00000510286.1:c.53A>C ENSP00000427268.1:p.Asn18Thr
NM_001347.3:c.278A>C NP_001338.2:p.Asn93Thr
XM_011513411.1:c.278A>C XP_011511713.1:p.Asn93Thr
XM_011513412.1:c.278A>C XP_011511714.1:p.Asn93Thr
XM_011513413.1:c.278A>C XP_011511715.1:p.Asn93Thr
XM_011513414.1:c.278A>C XP_011511716.1:p.Asn93Thr
XM_011513415.1:c.278A>C XP_011511717.1:p.Asn93Thr
XM_011513414.2:c.278A>C XP_011511716.1:p.Asn93Thr
XM_017007814.1:c.278A>C XP_016863303.1:p.Asn93Thr
XM_017007815.1:c.278A>C XP_016863304.1:p.Asn93Thr
XR_002959715.1:n.341A>C
NM_001347.4:c.278A>C MANE Select NP_001338.2:p.Asn93Thr