Canonical Allele Identifier: CA2087161036
Gene: DGKH HGNC NCBI

Linked Data

dbSNP Id: rs1954157601

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42079306_42079312del , CM000675.2:g.42079306_42079312del GRCh38
NC_000013.10:g.42653442_42653448del , CM000675.1:g.42653442_42653448del GRCh37
NC_000013.9:g.41551442_41551448del NCBI36
NG_029191.2:g.44271_44277del
NG_029191.3:g.44271_44277del

Transcript Alleles

HGVS Amino-acid change
ENST00000337343.9:c.192+30341_192+30347del MANE Select ENSP00000337572.4:n.192+30341_192+30347de...
ENST00000261491.9:c.192+30341_192+30347del ENSP00000261491.4:n.192+30341_192+30347de...
ENST00000337343.8:c.192+30341_192+30347del ENSP00000337572.4:n.192+30341_192+30347de...
ENST00000379274.6:c.192+30341_192+30347del ENSP00000368576.3:n.192+30341_192+30347de...
NM_001204504.2:c.192+30341_192+30347del NP_001191433.1:n.192+30341_192+30347del
NM_152910.5:c.192+30341_192+30347del NP_690874.2:n.192+30341_192+30347del
NM_178009.4:c.192+30341_192+30347del NP_821077.1:n.192+30341_192+30347del
NM_152910.6:c.192+30341_192+30347del NP_690874.2:n.192+30341_192+30347del
NM_178009.5:c.192+30341_192+30347del MANE Select NP_821077.1:n.192+30341_192+30347del
NM_001204504.3:c.192+30341_192+30347del NP_001191433.1:n.192+30341_192+30347del