Canonical Allele Identifier: CA1968785778

Gene: DGKZ

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46357892T>G , CM000673.2:g.46357892T>G	GRCh38
NC_000011.9:g.46379442T>G , CM000673.1:g.46379442T>G	GRCh37
NC_000011.8:g.46336018T>G	NCBI36
NG_047092.1:g.29988T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456247.7:c.162-9399T>G MANE Select	ENSP00000395684.2:n.162-9399T>G
ENST00000318201.12:c.162-9399T>G	ENSP00000320340.8:n.162-9399T>G
ENST00000343674.10:c.213-9399T>G	ENSP00000343065.6:n.213-9399T>G
ENST00000421244.6:c.162-9399T>G	ENSP00000391021.2:n.162-9399T>G
ENST00000456247.6:c.162-9399T>G	ENSP00000395684.2:n.162-9399T>G
ENST00000524984.5:c.60-9399T>G	ENSP00000437060.1:n.60-9399T>G
ENST00000525242.5:c.-199-9399T>G	ENSP00000435332.1:n.-199-9399T>G
ENST00000527674.5:n.153-9399T>G
ENST00000527911.5:c.162-9399T>G	ENSP00000436291.1:n.162-9399T>G
ENST00000528615.5:c.-222-11602T>G	ENSP00000434719.1:n.-222-11602T>G
ENST00000531879.5:n.155-9399T>G
ENST00000532868.6:c.177-9399T>G	ENSP00000436273.2:n.177-9399T>G
ENST00000533376.5:c.161+10072T>G	ENSP00000435435.1:n.161+10072T>G
NM_001199266.1:c.162-9399T>G	NP_001186195.1:n.162-9399T>G
NM_001199267.1:c.162-9399T>G	NP_001186196.1:n.162-9399T>G
NM_001199268.1:c.162-9399T>G	NP_001186197.1:n.162-9399T>G
NM_003646.3:c.162-9399T>G	NP_003637.2:n.162-9399T>G
NM_201532.2:c.213-9399T>G	NP_963290.1:n.213-9399T>G
NM_201533.3:c.177-9399T>G	NP_963291.2:n.177-9399T>G
XM_005253181.3:c.213-9399T>G	XP_005253238.1:n.213-9399T>G
XM_005253182.3:c.177-9399T>G	XP_005253239.1:n.177-9399T>G
XM_006718355.2:c.177-9399T>G	XP_006718418.1:n.177-9399T>G
XM_011520422.1:c.177-9399T>G	XP_011518724.1:n.177-9399T>G
XM_011520423.1:c.-199-9399T>G	XP_011518725.1:n.-199-9399T>G
XM_017018455.1:c.162-8352T>G	XP_016873944.1:n.162-8352T>G
XM_017018456.1:c.162-8352T>G	XP_016873945.1:n.162-8352T>G
XM_024448729.1:c.162-8352T>G	XP_024304497.1:n.162-8352T>G
XM_024448730.1:c.162-8352T>G	XP_024304498.1:n.162-8352T>G
XM_024448731.1:c.162-8352T>G	XP_024304499.1:n.162-8352T>G
XM_024448733.1:c.213-9399T>G	XP_024304501.1:n.213-9399T>G
XM_024448734.1:c.213-9399T>G	XP_024304502.1:n.213-9399T>G
XM_024448735.1:c.177-9399T>G	XP_024304503.1:n.177-9399T>G
XM_024448736.1:c.177-9399T>G	XP_024304504.1:n.177-9399T>G
XM_024448737.1:c.162-9399T>G	XP_024304505.1:n.162-9399T>G
XM_024448738.1:c.162-9399T>G	XP_024304506.1:n.162-9399T>G
XM_024448739.1:c.177-9399T>G	XP_024304507.1:n.177-9399T>G
XM_024448740.1:c.177-9399T>G	XP_024304508.1:n.177-9399T>G
XM_024448741.1:c.-199-9399T>G	XP_024304509.1:n.-199-9399T>G
XR_002957206.1:n.273-8352T>G
NM_001199266.2:c.162-9399T>G	NP_001186195.1:n.162-9399T>G
NM_001199267.2:c.162-9399T>G MANE Select	NP_001186196.1:n.162-9399T>G
NM_001199268.2:c.162-9399T>G	NP_001186197.1:n.162-9399T>G
NM_003646.4:c.162-9399T>G	NP_003637.2:n.162-9399T>G
NM_201532.3:c.213-9399T>G	NP_963290.1:n.213-9399T>G