Canonical Allele Identifier: CA800427931

Gene: DGKQ

Linked Data

• dbSNP Id: rs1288989722
• MyVariant Identifiers: chr4:g.964451_964452insA (hg19) ; chr4:g.970663_970664insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.970664dup , CM000666.2:g.970664dup	GRCh38
NC_000004.11:g.964452dup , CM000666.1:g.964452dup	GRCh37
NC_000004.10:g.954452dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000273814.8:c.351+329dup MANE Select	ENSP00000273814.3:n.351+329dup
ENST00000273814.7:c.351+329dup	ENSP00000273814.3:n.351+329dup
ENST00000509465.5:c.191+329dup
ENST00000510286.1:c.126+329dup	ENSP00000427268.1:n.126+329dup
NM_001347.3:c.351+329dup	NP_001338.2:n.351+329dup
XM_011513411.1:c.351+329dup	XP_011511713.1:n.351+329dup
XM_011513412.1:c.351+329dup	XP_011511714.1:n.351+329dup
XM_011513413.1:c.351+329dup	XP_011511715.1:n.351+329dup
XM_011513414.1:c.351+329dup	XP_011511716.1:n.351+329dup
XM_011513415.1:c.351+329dup	XP_011511717.1:n.351+329dup
XM_011513414.2:c.351+329dup	XP_011511716.1:n.351+329dup
XM_017007814.1:c.351+329dup	XP_016863303.1:n.351+329dup
XM_017007815.1:c.351+329dup	XP_016863304.1:n.351+329dup
XR_002959715.1:n.414+329dup
NM_001347.4:c.351+329dup MANE Select	NP_001338.2:n.351+329dup