Canonical Allele Identifier: CA1335702369

Gene: DGKD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233356202C= , CM000664.2:g.233356202C=	GRCh38
NC_000002.11:g.234264848C= , CM000664.1:g.234264848C=	GRCh37
NC_000002.10:g.233929587C=	NCBI36
NG_029495.1:g.6696C=

Transcript Alleles

HGVS	Amino-acid Change
NM_152879.3:c.156+1528C= MANE Select	NP_690618.2:n.156+1528C=
ENST00000264057.7:c.156+1528C= MANE Select	ENSP00000264057.2:n.156+1528C=
NM_152879.2:c.156+1528C=	NP_690618.2:n.156+1528C=
ENST00000264057.6:c.156+1528C=	ENSP00000264057.2:n.156+1528C=
ENST00000427930.5:c.156+1528C=	ENSP00000407938.1:n.156+1528C=
ENST00000442524.4:c.103+1528C=
XM_011512028.3:c.-894C=	XP_011510330.1:n.-894C=
XM_011512029.3:c.-894C=	XP_011510331.1:n.-894C=
XM_011512033.3:c.-894C=	XP_011510335.1:n.-894C=
XM_011512036.1:c.36+543C=	XP_011510338.1:n.36+543C=
XM_011512039.2:c.-894C=	XP_011510341.1:n.-894C=
XM_017005138.2:c.36+543C=	XP_016860627.1:n.36+543C=
XR_923050.2:n.512C=