Canonical Allele Identifier: CA2087195564
Gene: DGKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42160691C= , CM000675.2:g.42160691C= GRCh38
NC_000013.10:g.42734827C= , CM000675.1:g.42734827C= GRCh37
NC_000013.9:g.41632827C= NCBI36
NG_029191.2:g.125656C=
NG_029191.3:g.125656C=

Transcript Alleles

HGVS Amino-acid change
ENST00000337343.9:c.855+555C= MANE Select ENSP00000337572.4:n.855+555C=
ENST00000261491.9:c.855+555C= ENSP00000261491.4:n.855+555C=
ENST00000337343.8:c.855+555C= ENSP00000337572.4:n.855+555C=
ENST00000379274.6:c.855+555C= ENSP00000368576.3:n.855+555C=
ENST00000498255.6:n.1086+555C=
ENST00000536612.3:c.447+555C= ENSP00000445114.2:n.447+555C=
ENST00000626247.2:c.215-4640C= ENSP00000486329.1:n.215-4640C=
ENST00000627777.2:c.447+555C= ENSP00000486838.1:n.447+555C=
ENST00000628433.2:c.447+555C= ENSP00000485809.1:n.447+555C=
NM_001204504.2:c.855+555C= NP_001191433.1:n.855+555C=
NM_001204505.2:c.447+555C= NP_001191434.1:n.447+555C=
NM_001204506.2:c.447+555C= NP_001191435.1:n.447+555C=
NM_001297429.1:c.121-4640C= NP_001284358.1:n.121-4640C=
NM_152910.5:c.855+555C= NP_690874.2:n.855+555C=
NM_178009.4:c.855+555C= NP_821077.1:n.855+555C=
NR_123714.1:n.579+555C=
NR_123715.1:n.1192+555C=
NM_001204505.3:c.447+555C= NP_001191434.1:n.447+555C=
NM_001204506.3:c.447+555C= NP_001191435.1:n.447+555C=
NM_001297429.2:c.121-4640C= NP_001284358.1:n.121-4640C=
NM_152910.6:c.855+555C= NP_690874.2:n.855+555C=
NM_178009.5:c.855+555C= MANE Select NP_821077.1:n.855+555C=
NR_123714.2:n.563+555C=
NR_123715.2:n.1176+555C=
NM_001204504.3:c.855+555C= NP_001191433.1:n.855+555C=