Canonical Allele Identifier: CA5963384
Community Standard Title: NM_001199267.2(DGKZ):c.2660C>G (p.Thr887Arg)
Gene: DGKZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46379558C>G , CM000673.2:g.46379558C>G GRCh38
NC_000011.9:g.46401108C>G , CM000673.1:g.46401108C>G GRCh37
NC_000011.8:g.46357684C>G NCBI36
NG_047092.1:g.51654C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001199267.2:c.2660C>G MANE Select NP_001186196.1:p.Thr887Arg
ENST00000456247.7:c.2660C>G MANE Select ENSP00000395684.2:p.Thr887Arg
NM_001105540.1:c.3227C>G NP_001099010.1:p.Thr1076Arg
NM_001105540.2:c.3227C>G NP_001099010.1:p.Thr1076Arg
NM_001199266.1:c.2678C>G NP_001186195.1:p.Thr893Arg
NM_001199266.2:c.2678C>G NP_001186195.1:p.Thr893Arg
NM_001199267.1:c.2660C>G NP_001186196.1:p.Thr887Arg
NM_001199268.1:c.2594C>G NP_001186197.1:p.Thr865Arg
NM_001199268.2:c.2594C>G NP_001186197.1:p.Thr865Arg
NM_003646.3:c.2663C>G NP_003637.2:p.Thr888Arg
NM_003646.4:c.2663C>G NP_003637.2:p.Thr888Arg
NM_201532.2:c.2711C>G NP_963290.1:p.Thr904Arg
NM_201532.3:c.2711C>G NP_963290.1:p.Thr904Arg
NM_201533.3:c.2675C>G NP_963291.2:p.Thr892Arg
ENST00000318201.12:c.2594C>G ENSP00000320340.8:p.Thr865Arg
ENST00000343674.10:c.2711C>G ENSP00000343065.6:p.Thr904Arg
ENST00000421244.6:c.2663C>G ENSP00000391021.2:p.Thr888Arg
ENST00000454345.5:c.3227C>G ENSP00000412178.1:p.Thr1076Arg
ENST00000454345.6:c.3227C>G ENSP00000412178.1:p.Thr1076Arg
ENST00000456247.6:c.2660C>G ENSP00000395684.2:p.Thr887Arg
ENST00000524984.5:c.*2280C>G ENSP00000437060.1:n.*2280C>G
ENST00000527211.5:n.2948C>G
ENST00000527911.5:c.2678C>G ENSP00000436291.1:p.Thr893Arg
ENST00000528173.5:n.5004C>G
ENST00000528615.5:c.1997C>G ENSP00000434719.1:p.Thr666Arg
ENST00000529660.5:n.483C>G
ENST00000532868.6:c.2675C>G ENSP00000436273.2:p.Thr892Arg
ENST00000534802.1:n.1268C>G
XM_005253181.3:c.2714C>G XP_005253238.1:p.Thr905Arg
XM_005253182.3:c.2678C>G XP_005253239.1:p.Thr893Arg
XM_006718354.1:c.3230C>G XP_006718417.1:p.Thr1077Arg
XM_006718355.2:c.2675C>G XP_006718418.1:p.Thr892Arg
XM_011520421.1:c.3290C>G XP_011518723.1:p.Thr1097Arg
XM_011520422.1:c.2609C>G XP_011518724.1:p.Thr870Arg
XM_011520423.1:c.2303C>G XP_011518725.1:p.Thr768Arg
XM_017018455.1:c.3404C>G XP_016873944.1:p.Thr1135Arg
XM_017018456.1:c.3401C>G XP_016873945.1:p.Thr1134Arg
XM_024448729.1:c.3503C>G XP_024304497.1:p.Thr1168Arg
XM_024448730.1:c.3500C>G XP_024304498.1:p.Thr1167Arg
XM_024448731.1:c.3434C>G XP_024304499.1:p.Thr1145Arg
XM_024448732.1:c.3329C>G XP_024304500.1:p.Thr1110Arg
XM_024448733.1:c.2813C>G XP_024304501.1:p.Thr938Arg
XM_024448734.1:c.2810C>G XP_024304502.1:p.Thr937Arg
XM_024448735.1:c.2777C>G XP_024304503.1:p.Thr926Arg
XM_024448736.1:c.2774C>G XP_024304504.1:p.Thr925Arg
XM_024448737.1:c.2762C>G XP_024304505.1:p.Thr921Arg
XM_024448738.1:c.2759C>G XP_024304506.1:p.Thr920Arg
XM_024448739.1:c.2708C>G XP_024304507.1:p.Thr903Arg
XM_024448741.1:c.2402C>G XP_024304509.1:p.Thr801Arg
XR_002957206.1:n.3711C>G
XR_930918.1:n.6910C>G