Canonical Allele Identifier: CA1433035333
Gene: DGKQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.970394_970399delinsAGAAGG , CM000666.2:g.970394_970399delinsAGAAGG GRCh38
NC_000004.11:g.964182_964187delinsAGAAGG , CM000666.1:g.964182_964187delinsAGAAGG GRCh37
NC_000004.10:g.954182_954187delinsAGAAGG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000273814.8:c.351+594_351+599delinsCCTTCT MANE Select ENSP00000273814.3:n.351+594_351+599delins...
ENST00000273814.7:c.351+594_351+599delinsCCTTCT ENSP00000273814.3:n.351+594_351+599delins...
ENST00000509465.5:c.191+594_191+599delinsCCTTCT
ENST00000510286.1:c.126+594_126+599delinsCCTTCT ENSP00000427268.1:n.126+594_126+599delins...
NM_001347.3:c.351+594_351+599delinsCCTTCT NP_001338.2:n.351+594_351+599delinsCCTTCT...
XM_011513411.1:c.351+594_351+599delinsCCTTCT XP_011511713.1:n.351+594_351+599delinsCCT...
XM_011513412.1:c.351+594_351+599delinsCCTTCT XP_011511714.1:n.351+594_351+599delinsCCT...
XM_011513413.1:c.351+594_351+599delinsCCTTCT XP_011511715.1:n.351+594_351+599delinsCCT...
XM_011513414.1:c.351+594_351+599delinsCCTTCT XP_011511716.1:n.351+594_351+599delinsCCT...
XM_011513415.1:c.351+594_351+599delinsCCTTCT XP_011511717.1:n.351+594_351+599delinsCCT...
XM_011513414.2:c.351+594_351+599delinsCCTTCT XP_011511716.1:n.351+594_351+599delinsCCT...
XM_017007814.1:c.351+594_351+599delinsCCTTCT XP_016863303.1:n.351+594_351+599delinsCCT...
XM_017007815.1:c.351+594_351+599delinsCCTTCT XP_016863304.1:n.351+594_351+599delinsCCT...
XR_002959715.1:n.414+594_414+599delinsCCTTCT
NM_001347.4:c.351+594_351+599delinsCCTTCT MANE Select NP_001338.2:n.351+594_351+599delinsCCTTCT...