Canonical Allele Identifier: CA698146399

Gene: DGKH

Linked Data

• dbSNP Id: rs1338424844
• MyVariant Identifiers: chr13:g.42653488C>G (hg19) ; chr13:g.42079352C>G (hg38)

Genomic Alleles

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

Transcript Alleles

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