Canonical Allele Identifier: CA2087161062
Gene: DGKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42079364G= , CM000675.2:g.42079364G= GRCh38
NC_000013.10:g.42653500G= , CM000675.1:g.42653500G= GRCh37
NC_000013.9:g.41551500G= NCBI36
NG_029191.2:g.44329G=
NG_029191.3:g.44329G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337343.9:c.192+30399G= MANE Select ENSP00000337572.4:n.192+30399G=
ENST00000261491.9:c.192+30399G= ENSP00000261491.4:n.192+30399G=
ENST00000337343.8:c.192+30399G= ENSP00000337572.4:n.192+30399G=
ENST00000379274.6:c.192+30399G= ENSP00000368576.3:n.192+30399G=
NM_001204504.2:c.192+30399G= NP_001191433.1:n.192+30399G=
NM_152910.5:c.192+30399G= NP_690874.2:n.192+30399G=
NM_178009.4:c.192+30399G= NP_821077.1:n.192+30399G=
NM_152910.6:c.192+30399G= NP_690874.2:n.192+30399G=
NM_178009.5:c.192+30399G= MANE Select NP_821077.1:n.192+30399G=
NM_001204504.3:c.192+30399G= NP_001191433.1:n.192+30399G=