Canonical Allele Identifier: CA2087195640
Gene: DGKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42160871G= , CM000675.2:g.42160871G= GRCh38
NC_000013.10:g.42735007G= , CM000675.1:g.42735007G= GRCh37
NC_000013.9:g.41633007G= NCBI36
NG_029191.2:g.125836G=
NG_029191.3:g.125836G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337343.9:c.855+735G= MANE Select ENSP00000337572.4:n.855+735G=
ENST00000261491.9:c.855+735G= ENSP00000261491.4:n.855+735G=
ENST00000337343.8:c.855+735G= ENSP00000337572.4:n.855+735G=
ENST00000379274.6:c.855+735G= ENSP00000368576.3:n.855+735G=
ENST00000498255.6:n.1086+735G=
ENST00000536612.3:c.447+735G= ENSP00000445114.2:n.447+735G=
ENST00000626247.2:c.215-4460G= ENSP00000486329.1:n.215-4460G=
ENST00000627777.2:c.447+735G= ENSP00000486838.1:n.447+735G=
ENST00000628433.2:c.447+735G= ENSP00000485809.1:n.447+735G=
NM_001204504.2:c.855+735G= NP_001191433.1:n.855+735G=
NM_001204505.2:c.447+735G= NP_001191434.1:n.447+735G=
NM_001204506.2:c.447+735G= NP_001191435.1:n.447+735G=
NM_001297429.1:c.121-4460G= NP_001284358.1:n.121-4460G=
NM_152910.5:c.855+735G= NP_690874.2:n.855+735G=
NM_178009.4:c.855+735G= NP_821077.1:n.855+735G=
NR_123714.1:n.579+735G=
NR_123715.1:n.1192+735G=
NM_001204505.3:c.447+735G= NP_001191434.1:n.447+735G=
NM_001204506.3:c.447+735G= NP_001191435.1:n.447+735G=
NM_001297429.2:c.121-4460G= NP_001284358.1:n.121-4460G=
NM_152910.6:c.855+735G= NP_690874.2:n.855+735G=
NM_178009.5:c.855+735G= MANE Select NP_821077.1:n.855+735G=
NR_123714.2:n.563+735G=
NR_123715.2:n.1176+735G=
NM_001204504.3:c.855+735G= NP_001191433.1:n.855+735G=