Canonical Allele Identifier: CA437908065

Gene: DGKQ

Linked Data

• MyVariant Identifiers: chr4:g.964796T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.971008T>G , CM000666.2:g.971008T>G	GRCh38
NC_000004.11:g.964796T>G , CM000666.1:g.964796T>G	GRCh37
NC_000004.10:g.954796T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273814.8:c.336A>C MANE Select	ENSP00000273814.3:p.Ala112=
ENST00000273814.7:c.336A>C	ENSP00000273814.3:p.Ala112=
ENST00000509465.5:c.176A>C
ENST00000510286.1:c.111A>C	ENSP00000427268.1:p.Ala37=
NM_001347.3:c.336A>C	NP_001338.2:p.Ala112=
XM_011513411.1:c.336A>C	XP_011511713.1:p.Ala112=
XM_011513412.1:c.336A>C	XP_011511714.1:p.Ala112=
XM_011513413.1:c.336A>C	XP_011511715.1:p.Ala112=
XM_011513414.1:c.336A>C	XP_011511716.1:p.Ala112=
XM_011513415.1:c.336A>C	XP_011511717.1:p.Ala112=
XM_011513414.2:c.336A>C	XP_011511716.1:p.Ala112=
XM_017007814.1:c.336A>C	XP_016863303.1:p.Ala112=
XM_017007815.1:c.336A>C	XP_016863304.1:p.Ala112=
XR_002959715.1:n.399A>C
NM_001347.4:c.336A>C MANE Select	NP_001338.2:p.Ala112=