Canonical Allele Identifier: CA2157122285
Gene: VRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.96876079C= , CM000676.2:g.96876079C= GRCh38
NC_000014.8:g.97342416C= , CM000676.1:g.97342416C= GRCh37
NC_000014.7:g.96412169C= NCBI36
NG_016293.1:g.83733C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216639.8:c.1118C= MANE Select ENSP00000216639.3:p.Thr373=
ENST00000553683.2:c.1118C= ENSP00000451412.2:p.Thr373=
ENST00000555067.2:n.11172C=
ENST00000679365.1:c.1109C= ENSP00000505882.1:p.Thr370=
ENST00000679462.1:c.1153C= ENSP00000506011.1:p.Arg385=
ENST00000679506.1:n.3177C=
ENST00000679533.1:c.*891C= ENSP00000505873.1:n.*891C=
ENST00000679650.1:c.*807C= ENSP00000505156.1:n.*807C=
ENST00000679727.1:c.1112C= ENSP00000505844.1:p.Thr371=
ENST00000679758.1:c.1068+15344C= ENSP00000505539.1:n.1068+15344C=
ENST00000679770.1:c.1118C= ENSP00000505214.1:p.Thr373=
ENST00000679816.1:c.1118C= ENSP00000506525.1:p.Thr373=
ENST00000679843.1:c.421C= ENSP00000506467.1:n.421C=
ENST00000679903.1:c.1109C= ENSP00000506022.1:p.Thr370=
ENST00000679918.1:c.1118C= ENSP00000505439.1:p.Thr373=
ENST00000679941.1:c.1068+15344C= ENSP00000506520.1:n.1068+15344C=
ENST00000679977.1:c.*364C= ENSP00000504897.1:n.*364C=
ENST00000680007.1:c.1118C= ENSP00000505683.1:p.Thr373=
ENST00000680335.1:c.1068+15344C= ENSP00000505806.1:n.1068+15344C=
ENST00000680387.1:c.1115C= ENSP00000504908.1:p.Thr372=
ENST00000680526.1:c.*587+15415C= ENSP00000505595.1:n.*587+15415C=
ENST00000680538.1:c.1028C= ENSP00000505611.1:p.Thr343=
ENST00000680683.1:c.1118C= ENSP00000506334.1:p.Thr373=
ENST00000680724.1:c.1118C= ENSP00000504891.1:p.Thr373=
ENST00000680756.1:c.1118C= ENSP00000506648.1:p.Thr373=
ENST00000680849.1:c.1115C= ENSP00000505602.1:p.Thr372=
ENST00000680851.1:c.1069-5098C= ENSP00000505159.1:n.1069-5098C=
ENST00000680922.1:c.*212+15344C= ENSP00000506480.1:n.*212+15344C=
ENST00000680993.1:c.*432+15344C= ENSP00000505511.1:n.*432+15344C=
ENST00000681061.1:c.692+15344C=
ENST00000681101.1:c.1118C= ENSP00000506564.1:p.Thr373=
ENST00000681195.1:c.1115C= ENSP00000504933.1:p.Thr372=
ENST00000681249.1:c.1115C= ENSP00000506013.1:p.Thr372=
ENST00000681344.1:c.1118C= ENSP00000506151.1:p.Thr373=
ENST00000681355.1:c.1118C= ENSP00000506214.1:p.Thr373=
ENST00000681363.1:c.*218C= ENSP00000505564.1:n.*218C=
ENST00000681419.1:c.1118C= ENSP00000505512.1:p.Thr373=
ENST00000681474.1:c.*30C= ENSP00000505569.1:n.*30C=
ENST00000681493.1:c.1112C= ENSP00000506429.1:p.Thr371=
ENST00000681524.1:c.*262C= ENSP00000505783.1:n.*262C=
ENST00000681538.1:c.*287C= ENSP00000506662.1:n.*287C=
ENST00000681598.1:c.*537+15344C= ENSP00000506128.1:n.*537+15344C=
ENST00000681677.1:c.742C=
ENST00000681695.1:c.*708C= ENSP00000506225.1:n.*708C=
ENST00000681778.1:c.1068+15344C= ENSP00000506049.1:n.1068+15344C=
ENST00000216639.7:c.1118C= ENSP00000216639.3:p.Thr373=
ENST00000553683.1:c.51C=
ENST00000555067.1:n.348C=
ENST00000557222.5:c.637+15344C=
NM_003384.2:c.1118C= NP_003375.1:p.Thr373=
XM_006720247.2:c.1118C= XP_006720310.1:p.Thr373=
XM_011537132.1:c.1115C= XP_011535434.1:p.Thr372=
XM_006720247.4:c.1118C= XP_006720310.1:p.Thr373=
XM_017021624.2:c.1115C= XP_016877113.1:p.Thr372=
XM_017021625.1:c.1124C= XP_016877114.1:p.Thr375=
XR_001750539.2:n.1065C=
NM_003384.3:c.1118C= MANE Select NP_003375.1:p.Thr373=