Canonical Allele Identifier: CA698155800
Gene: DGKH HGNC NCBI

Linked Data

dbSNP Id: rs1238359684

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42101314A>G , CM000675.2:g.42101314A>G GRCh38
NC_000013.10:g.42675450A>G , CM000675.1:g.42675450A>G GRCh37
NC_000013.9:g.41573450A>G NCBI36
NG_029191.2:g.66279A>G
NG_029191.3:g.66279A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000337343.9:c.193-26149A>G MANE Select ENSP00000337572.4:n.193-26149A>G
ENST00000261491.9:c.193-26149A>G ENSP00000261491.4:n.193-26149A>G
ENST00000337343.8:c.193-26149A>G ENSP00000337572.4:n.193-26149A>G
ENST00000379274.6:c.193-26149A>G ENSP00000368576.3:n.193-26149A>G
NM_001204504.2:c.193-26149A>G NP_001191433.1:n.193-26149A>G
NM_152910.5:c.193-26149A>G NP_690874.2:n.193-26149A>G
NM_178009.4:c.193-26149A>G NP_821077.1:n.193-26149A>G
NM_152910.6:c.193-26149A>G NP_690874.2:n.193-26149A>G
NM_178009.5:c.193-26149A>G MANE Select NP_821077.1:n.193-26149A>G
NM_001204504.3:c.193-26149A>G NP_001191433.1:n.193-26149A>G