Canonical Allele Identifier: CA2087224942

Gene: DGKH

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42229033A= , CM000675.2:g.42229033A=	GRCh38
NC_000013.10:g.42803169A= , CM000675.1:g.42803169A=	GRCh37
NC_000013.9:g.41701169A=	NCBI36
NG_029191.2:g.193998A=
NG_029191.3:g.193998A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000337343.9:c.3574-66A= MANE Select	ENSP00000337572.4:n.3574-66A=
ENST00000261491.9:c.3443-66A=	ENSP00000261491.4:n.3443-66A=
ENST00000337343.8:c.3574-66A=	ENSP00000337572.4:n.3574-66A=
ENST00000379274.6:c.3443-66A=	ENSP00000368576.3:n.3443-66A=
ENST00000498255.6:n.3869-66A=
ENST00000536612.3:c.3214-66A=	ENSP00000445114.2:n.3214-66A=
ENST00000626247.2:c.*2532-66A=	ENSP00000486329.1:n.*2532-66A=
ENST00000627777.2:c.*181-66A=	ENSP00000486838.1:n.*181-66A=
ENST00000628433.2:c.3166-66A=	ENSP00000485809.1:n.3166-66A=
NM_001204504.2:c.3443-66A=	NP_001191433.1:n.3443-66A=
NM_001204505.2:c.3214-66A=	NP_001191434.1:n.3214-66A=
NM_001204506.2:c.3166-66A=	NP_001191435.1:n.3166-66A=
NM_001297429.1:c.2708-66A=	NP_001284358.1:n.2708-66A=
NM_152910.5:c.3443-66A=	NP_690874.2:n.3443-66A=
NM_178009.4:c.3574-66A=	NP_821077.1:n.3574-66A=
NR_123714.1:n.3400-66A=
NR_123715.1:n.3975-66A=
NM_001204505.3:c.3214-66A=	NP_001191434.1:n.3214-66A=
NM_001204506.3:c.3166-66A=	NP_001191435.1:n.3166-66A=
NM_001297429.2:c.2708-66A=	NP_001284358.1:n.2708-66A=
NM_152910.6:c.3443-66A=	NP_690874.2:n.3443-66A=
NM_178009.5:c.3574-66A= MANE Select	NP_821077.1:n.3574-66A=
NR_123714.2:n.3384-66A=
NR_123715.2:n.3959-66A=
NM_001204504.3:c.3443-66A=	NP_001191433.1:n.3443-66A=