Canonical Allele Identifier: CA2798963616
Gene: DGKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42101503del , CM000675.2:g.42101503del GRCh38
NC_000013.10:g.42675639del , CM000675.1:g.42675639del GRCh37
NC_000013.9:g.41573639del NCBI36
NG_029191.2:g.66468del
NG_029191.3:g.66468del

Transcript Alleles

HGVS Amino-acid change
ENST00000337343.9:c.193-25960del MANE Select ENSP00000337572.4:n.193-25960del
ENST00000261491.9:c.193-25960del ENSP00000261491.4:n.193-25960del
ENST00000337343.8:c.193-25960del ENSP00000337572.4:n.193-25960del
ENST00000379274.6:c.193-25960del ENSP00000368576.3:n.193-25960del
NM_001204504.2:c.193-25960del NP_001191433.1:n.193-25960del
NM_152910.5:c.193-25960del NP_690874.2:n.193-25960del
NM_178009.4:c.193-25960del NP_821077.1:n.193-25960del
NM_152910.6:c.193-25960del NP_690874.2:n.193-25960del
NM_178009.5:c.193-25960del MANE Select NP_821077.1:n.193-25960del
NM_001204504.3:c.193-25960del NP_001191433.1:n.193-25960del