Canonical Allele Identifier: CA698155836

Gene: DGKH

Linked Data

• dbSNP Id: rs1216555431
• MyVariant Identifiers: chr13:g.42675592_42675593del (hg19) ; chr13:g.42101456_42101457del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42101456_42101457del , CM000675.2:g.42101456_42101457del	GRCh38
NC_000013.10:g.42675592_42675593del , CM000675.1:g.42675592_42675593del	GRCh37
NC_000013.9:g.41573592_41573593del	NCBI36
NG_029191.2:g.66421_66422del
NG_029191.3:g.66421_66422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337343.9:c.193-26007_193-26006del MANE Select	ENSP00000337572.4:n.193-26007_193-26006del
ENST00000261491.9:c.193-26007_193-26006del	ENSP00000261491.4:n.193-26007_193-26006del
ENST00000337343.8:c.193-26007_193-26006del	ENSP00000337572.4:n.193-26007_193-26006del
ENST00000379274.6:c.193-26007_193-26006del	ENSP00000368576.3:n.193-26007_193-26006del
NM_001204504.2:c.193-26007_193-26006del	NP_001191433.1:n.193-26007_193-26006del
NM_152910.5:c.193-26007_193-26006del	NP_690874.2:n.193-26007_193-26006del
NM_178009.4:c.193-26007_193-26006del	NP_821077.1:n.193-26007_193-26006del
NM_152910.6:c.193-26007_193-26006del	NP_690874.2:n.193-26007_193-26006del
NM_178009.5:c.193-26007_193-26006del MANE Select	NP_821077.1:n.193-26007_193-26006del
NM_001204504.3:c.193-26007_193-26006del	NP_001191433.1:n.193-26007_193-26006del