Canonical Allele Identifier: CA2087224950
Gene: DGKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42229052T= , CM000675.2:g.42229052T= GRCh38
NC_000013.10:g.42803188T= , CM000675.1:g.42803188T= GRCh37
NC_000013.9:g.41701188T= NCBI36
NG_029191.2:g.194017T=
NG_029191.3:g.194017T=

Transcript Alleles

HGVS Amino-acid change
ENST00000337343.9:c.3574-47T= MANE Select ENSP00000337572.4:n.3574-47T=
ENST00000261491.9:c.3443-47T= ENSP00000261491.4:n.3443-47T=
ENST00000337343.8:c.3574-47T= ENSP00000337572.4:n.3574-47T=
ENST00000379274.6:c.3443-47T= ENSP00000368576.3:n.3443-47T=
ENST00000498255.6:n.3869-47T=
ENST00000536612.3:c.3214-47T= ENSP00000445114.2:n.3214-47T=
ENST00000626247.2:c.*2532-47T= ENSP00000486329.1:n.*2532-47T=
ENST00000627777.2:c.*181-47T= ENSP00000486838.1:n.*181-47T=
ENST00000628433.2:c.3166-47T= ENSP00000485809.1:n.3166-47T=
NM_001204504.2:c.3443-47T= NP_001191433.1:n.3443-47T=
NM_001204505.2:c.3214-47T= NP_001191434.1:n.3214-47T=
NM_001204506.2:c.3166-47T= NP_001191435.1:n.3166-47T=
NM_001297429.1:c.2708-47T= NP_001284358.1:n.2708-47T=
NM_152910.5:c.3443-47T= NP_690874.2:n.3443-47T=
NM_178009.4:c.3574-47T= NP_821077.1:n.3574-47T=
NR_123714.1:n.3400-47T=
NR_123715.1:n.3975-47T=
NM_001204505.3:c.3214-47T= NP_001191434.1:n.3214-47T=
NM_001204506.3:c.3166-47T= NP_001191435.1:n.3166-47T=
NM_001297429.2:c.2708-47T= NP_001284358.1:n.2708-47T=
NM_152910.6:c.3443-47T= NP_690874.2:n.3443-47T=
NM_178009.5:c.3574-47T= MANE Select NP_821077.1:n.3574-47T=
NR_123714.2:n.3384-47T=
NR_123715.2:n.3959-47T=
NM_001204504.3:c.3443-47T= NP_001191433.1:n.3443-47T=