Canonical Allele Identifier: CA2087161057
Gene: DGKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42079352C= , CM000675.2:g.42079352C= GRCh38
NC_000013.10:g.42653488C= , CM000675.1:g.42653488C= GRCh37
NC_000013.9:g.41551488C= NCBI36
NG_029191.2:g.44317C=
NG_029191.3:g.44317C=

Transcript Alleles

HGVS Amino-acid change
ENST00000337343.9:c.192+30387C= MANE Select ENSP00000337572.4:n.192+30387C=
ENST00000261491.9:c.192+30387C= ENSP00000261491.4:n.192+30387C=
ENST00000337343.8:c.192+30387C= ENSP00000337572.4:n.192+30387C=
ENST00000379274.6:c.192+30387C= ENSP00000368576.3:n.192+30387C=
NM_001204504.2:c.192+30387C= NP_001191433.1:n.192+30387C=
NM_152910.5:c.192+30387C= NP_690874.2:n.192+30387C=
NM_178009.4:c.192+30387C= NP_821077.1:n.192+30387C=
NM_152910.6:c.192+30387C= NP_690874.2:n.192+30387C=
NM_178009.5:c.192+30387C= MANE Select NP_821077.1:n.192+30387C=
NM_001204504.3:c.192+30387C= NP_001191433.1:n.192+30387C=