Canonical Allele Identifier: CA955366915

Gene: DGKH

Linked Data

• gnomAD v3: 13-42160880-C-CTCGGTGGTCGCCGG
• gnomAD v4: 13-42160880-C-CTCGGTGGTCGCCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42160880_42160881insTCGGTGGTCGCCGG , CM000675.2:g.42160880_42160881insTCGGTGGTCGCCGG	GRCh38
NC_000013.10:g.42735016_42735017insTCGGTGGTCGCCGG , CM000675.1:g.42735016_42735017insTCGGTGGTCGCCGG	GRCh37
NC_000013.9:g.41633016_41633017insTCGGTGGTCGCCGG	NCBI36
NG_029191.2:g.125845_125846insTCGGTGGTCGCCGG
NG_029191.3:g.125845_125846insTCGGTGGTCGCCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337343.9:c.855+744_855+745insTCGGTGGTCGCCGG MANE Select	ENSP00000337572.4:n.855+744_855+745insTCGGTGGTCGCCGG
ENST00000261491.9:c.855+744_855+745insTCGGTGGTCGCCGG	ENSP00000261491.4:n.855+744_855+745insTCGGTGGTCGCCGG
ENST00000337343.8:c.855+744_855+745insTCGGTGGTCGCCGG	ENSP00000337572.4:n.855+744_855+745insTCGGTGGTCGCCGG
ENST00000379274.6:c.855+744_855+745insTCGGTGGTCGCCGG	ENSP00000368576.3:n.855+744_855+745insTCGGTGGTCGCCGG
ENST00000498255.6:n.1086+744_1086+745insTCGGTGGTCGCCGG
ENST00000536612.3:c.447+744_447+745insTCGGTGGTCGCCGG	ENSP00000445114.2:n.447+744_447+745insTCGGTGGTCGCCGG
ENST00000626247.2:c.215-4451_215-4450insTCGGTGGTCGCCGG	ENSP00000486329.1:n.215-4451_215-4450insTCGGTGGTCGCCGG
ENST00000627777.2:c.447+744_447+745insTCGGTGGTCGCCGG	ENSP00000486838.1:n.447+744_447+745insTCGGTGGTCGCCGG
ENST00000628433.2:c.447+744_447+745insTCGGTGGTCGCCGG	ENSP00000485809.1:n.447+744_447+745insTCGGTGGTCGCCGG
NM_001204504.2:c.855+744_855+745insTCGGTGGTCGCCGG	NP_001191433.1:n.855+744_855+745insTCGGTGGTCGCCGG
NM_001204505.2:c.447+744_447+745insTCGGTGGTCGCCGG	NP_001191434.1:n.447+744_447+745insTCGGTGGTCGCCGG
NM_001204506.2:c.447+744_447+745insTCGGTGGTCGCCGG	NP_001191435.1:n.447+744_447+745insTCGGTGGTCGCCGG
NM_001297429.1:c.121-4451_121-4450insTCGGTGGTCGCCGG	NP_001284358.1:n.121-4451_121-4450insTCGGTGGTCGCCGG
NM_152910.5:c.855+744_855+745insTCGGTGGTCGCCGG	NP_690874.2:n.855+744_855+745insTCGGTGGTCGCCGG
NM_178009.4:c.855+744_855+745insTCGGTGGTCGCCGG	NP_821077.1:n.855+744_855+745insTCGGTGGTCGCCGG
NR_123714.1:n.579+744_579+745insTCGGTGGTCGCCGG
NR_123715.1:n.1192+744_1192+745insTCGGTGGTCGCCGG
NM_001204505.3:c.447+744_447+745insTCGGTGGTCGCCGG	NP_001191434.1:n.447+744_447+745insTCGGTGGTCGCCGG
NM_001204506.3:c.447+744_447+745insTCGGTGGTCGCCGG	NP_001191435.1:n.447+744_447+745insTCGGTGGTCGCCGG
NM_001297429.2:c.121-4451_121-4450insTCGGTGGTCGCCGG	NP_001284358.1:n.121-4451_121-4450insTCGGTGGTCGCCGG
NM_152910.6:c.855+744_855+745insTCGGTGGTCGCCGG	NP_690874.2:n.855+744_855+745insTCGGTGGTCGCCGG
NM_178009.5:c.855+744_855+745insTCGGTGGTCGCCGG MANE Select	NP_821077.1:n.855+744_855+745insTCGGTGGTCGCCGG
NR_123714.2:n.563+744_563+745insTCGGTGGTCGCCGG
NR_123715.2:n.1176+744_1176+745insTCGGTGGTCGCCGG
NM_001204504.3:c.855+744_855+745insTCGGTGGTCGCCGG	NP_001191433.1:n.855+744_855+745insTCGGTGGTCGCCGG