Canonical Allele Identifier: CA2087170377
Gene: DGKH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42101480A= , CM000675.2:g.42101480A= GRCh38
NC_000013.10:g.42675616A= , CM000675.1:g.42675616A= GRCh37
NC_000013.9:g.41573616A= NCBI36
NG_029191.2:g.66445A=
NG_029191.3:g.66445A=

Transcript Alleles

HGVS Amino-acid change
ENST00000337343.9:c.193-25983A= MANE Select ENSP00000337572.4:n.193-25983A=
ENST00000261491.9:c.193-25983A= ENSP00000261491.4:n.193-25983A=
ENST00000337343.8:c.193-25983A= ENSP00000337572.4:n.193-25983A=
ENST00000379274.6:c.193-25983A= ENSP00000368576.3:n.193-25983A=
NM_001204504.2:c.193-25983A= NP_001191433.1:n.193-25983A=
NM_152910.5:c.193-25983A= NP_690874.2:n.193-25983A=
NM_178009.4:c.193-25983A= NP_821077.1:n.193-25983A=
NM_152910.6:c.193-25983A= NP_690874.2:n.193-25983A=
NM_178009.5:c.193-25983A= MANE Select NP_821077.1:n.193-25983A=
NM_001204504.3:c.193-25983A= NP_001191433.1:n.193-25983A=
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