Canonical Allele Identifier: CA1433035999

Gene: DGKQ

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.971023_971024delinsCG , CM000666.2:g.971023_971024delinsCG	GRCh38
NC_000004.11:g.964811_964812delinsCG , CM000666.1:g.964811_964812delinsCG	GRCh37
NC_000004.10:g.954811_954812delinsCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273814.8:c.320_321delinsCG MANE Select	ENSP00000273814.3:p.Pro107=
ENST00000273814.7:c.320_321delinsCG	ENSP00000273814.3:p.Pro107=
ENST00000509465.5:c.160_161delinsCG
ENST00000510286.1:c.95_96delinsCG	ENSP00000427268.1:p.Pro32=
NM_001347.3:c.320_321delinsCG	NP_001338.2:p.Pro107=
XM_011513411.1:c.320_321delinsCG	XP_011511713.1:p.Pro107=
XM_011513412.1:c.320_321delinsCG	XP_011511714.1:p.Pro107=
XM_011513413.1:c.320_321delinsCG	XP_011511715.1:p.Pro107=
XM_011513414.1:c.320_321delinsCG	XP_011511716.1:p.Pro107=
XM_011513415.1:c.320_321delinsCG	XP_011511717.1:p.Pro107=
XM_011513414.2:c.320_321delinsCG	XP_011511716.1:p.Pro107=
XM_017007814.1:c.320_321delinsCG	XP_016863303.1:p.Pro107=
XM_017007815.1:c.320_321delinsCG	XP_016863304.1:p.Pro107=
XR_002959715.1:n.383_384delinsCG
NM_001347.4:c.320_321delinsCG MANE Select	NP_001338.2:p.Pro107=