Canonical Allele Identifier: CA1433035507

Gene: DGKQ

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.970586G= , CM000666.2:g.970586G=	GRCh38
NC_000004.11:g.964374G= , CM000666.1:g.964374G=	GRCh37
NC_000004.10:g.954374G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000273814.8:c.351+407C= MANE Select	ENSP00000273814.3:n.351+407C=
ENST00000273814.7:c.351+407C=	ENSP00000273814.3:n.351+407C=
ENST00000509465.5:c.191+407C=
ENST00000510286.1:c.126+407C=	ENSP00000427268.1:n.126+407C=
NM_001347.3:c.351+407C=	NP_001338.2:n.351+407C=
XM_011513411.1:c.351+407C=	XP_011511713.1:n.351+407C=
XM_011513412.1:c.351+407C=	XP_011511714.1:n.351+407C=
XM_011513413.1:c.351+407C=	XP_011511715.1:n.351+407C=
XM_011513414.1:c.351+407C=	XP_011511716.1:n.351+407C=
XM_011513415.1:c.351+407C=	XP_011511717.1:n.351+407C=
XM_011513414.2:c.351+407C=	XP_011511716.1:n.351+407C=
XM_017007814.1:c.351+407C=	XP_016863303.1:n.351+407C=
XM_017007815.1:c.351+407C=	XP_016863304.1:n.351+407C=
XR_002959715.1:n.414+407C=
NM_001347.4:c.351+407C= MANE Select	NP_001338.2:n.351+407C=