Canonical Allele Identifier: CA2087170332

Gene: DGKH

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42101345T= , CM000675.2:g.42101345T=	GRCh38
NC_000013.10:g.42675481T= , CM000675.1:g.42675481T=	GRCh37
NC_000013.9:g.41573481T=	NCBI36
NG_029191.2:g.66310T=
NG_029191.3:g.66310T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337343.9:c.193-26118T= MANE Select	ENSP00000337572.4:n.193-26118T=
ENST00000261491.9:c.193-26118T=	ENSP00000261491.4:n.193-26118T=
ENST00000337343.8:c.193-26118T=	ENSP00000337572.4:n.193-26118T=
ENST00000379274.6:c.193-26118T=	ENSP00000368576.3:n.193-26118T=
NM_001204504.2:c.193-26118T=	NP_001191433.1:n.193-26118T=
NM_152910.5:c.193-26118T=	NP_690874.2:n.193-26118T=
NM_178009.4:c.193-26118T=	NP_821077.1:n.193-26118T=
NM_152910.6:c.193-26118T=	NP_690874.2:n.193-26118T=
NM_178009.5:c.193-26118T= MANE Select	NP_821077.1:n.193-26118T=
NM_001204504.3:c.193-26118T=	NP_001191433.1:n.193-26118T=