Canonical Allele Identifier: CA2580089056
Community Standard Title: NM_003384.3(VRK1):c.1144dup (p.Glu382GlyfsTer21)
Gene: VRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.96876105dup , CM000676.2:g.96876105dup GRCh38
NC_000014.8:g.97342442dup , CM000676.1:g.97342442dup GRCh37
NC_000014.7:g.96412195dup NCBI36
NG_016293.1:g.83759dup

Transcript Alleles

HGVS Amino-acid Change
NM_003384.3:c.1144dup MANE Select NP_003375.1:p.Glu382GlyfsTer21
ENST00000216639.8:c.1144dup MANE Select ENSP00000216639.3:p.Glu382GlyfsTer21
NM_003384.2:c.1144dup NP_003375.1:p.Glu382GlyfsTer21
ENST00000216639.7:c.1144dup ENSP00000216639.3:p.Glu382GlyfsTer21
ENST00000553683.1:c.77dup
ENST00000553683.2:c.1144dup ENSP00000451412.2:p.Glu382GlyfsTer8
ENST00000555067.1:n.374dup
ENST00000555067.2:n.11198dup
ENST00000557222.5:c.637+15370dup
ENST00000679365.1:c.1135dup ENSP00000505882.1:p.Glu379GlyfsTer10
ENST00000679462.1:c.1179dup ENSP00000506011.1:p.Arg394GlufsTer16
ENST00000679506.1:n.3203dup
ENST00000679533.1:c.*917dup ENSP00000505873.1:n.*917dup
ENST00000679650.1:c.*833dup ENSP00000505156.1:n.*833dup
ENST00000679727.1:c.1138dup ENSP00000505844.1:p.Glu380GlyfsTer21
ENST00000679758.1:c.1068+15370dup ENSP00000505539.1:n.1068+15370dup
ENST00000679770.1:c.1144dup ENSP00000505214.1:p.Glu382GlyfsTer?
ENST00000679816.1:c.1144dup ENSP00000506525.1:p.Glu382GlyfsTer21
ENST00000679843.1:c.447dup ENSP00000506467.1:n.447dup
ENST00000679903.1:c.1135dup ENSP00000506022.1:p.Glu379GlyfsTer21
ENST00000679918.1:c.1144dup ENSP00000505439.1:p.Glu382GlyfsTer8
ENST00000679941.1:c.1068+15370dup ENSP00000506520.1:n.1068+15370dup
ENST00000679977.1:c.*390dup ENSP00000504897.1:n.*390dup
ENST00000680007.1:c.1144dup ENSP00000505683.1:p.Glu382GlyfsTer8
ENST00000680335.1:c.1068+15370dup ENSP00000505806.1:n.1068+15370dup
ENST00000680387.1:c.1141dup ENSP00000504908.1:p.Glu381GlyfsTer10
ENST00000680526.1:c.*587+15441dup ENSP00000505595.1:n.*587+15441dup
ENST00000680538.1:c.1054dup ENSP00000505611.1:p.Glu352GlyfsTer21
ENST00000680683.1:c.1144dup ENSP00000506334.1:p.Glu382GlyfsTer28
ENST00000680724.1:c.1144dup ENSP00000504891.1:p.Glu382GlyfsTer14
ENST00000680756.1:c.1144dup ENSP00000506648.1:p.Glu382GlyfsTer21
ENST00000680849.1:c.1141dup ENSP00000505602.1:p.Glu381GlyfsTer21
ENST00000680851.1:c.1069-5072dup ENSP00000505159.1:n.1069-5072dup
ENST00000680922.1:c.*212+15370dup ENSP00000506480.1:n.*212+15370dup
ENST00000680993.1:c.*432+15370dup ENSP00000505511.1:n.*432+15370dup
ENST00000681061.1:c.692+15370dup
ENST00000681101.1:c.1144dup ENSP00000506564.1:p.Glu382GlyfsTer10
ENST00000681195.1:c.1141dup ENSP00000504933.1:p.Glu381GlyfsTer21
ENST00000681249.1:c.1141dup ENSP00000506013.1:p.Glu381GlyfsTer21
ENST00000681344.1:c.1144dup ENSP00000506151.1:p.Glu382GlyfsTer21
ENST00000681355.1:c.1144dup ENSP00000506214.1:p.Glu382GlyfsTer21
ENST00000681363.1:c.*244dup ENSP00000505564.1:n.*244dup
ENST00000681419.1:c.1144dup ENSP00000505512.1:p.Glu382GlyfsTer7
ENST00000681474.1:c.*56dup ENSP00000505569.1:n.*56dup
ENST00000681493.1:c.1138dup ENSP00000506429.1:p.Glu380GlyfsTer21
ENST00000681524.1:c.*288dup ENSP00000505783.1:n.*288dup
ENST00000681538.1:c.*313dup ENSP00000506662.1:n.*313dup
ENST00000681598.1:c.*537+15370dup ENSP00000506128.1:n.*537+15370dup
ENST00000681677.1:c.768dup
ENST00000681695.1:c.*734dup ENSP00000506225.1:n.*734dup
ENST00000681778.1:c.1068+15370dup ENSP00000506049.1:n.1068+15370dup
XM_006720247.2:c.1144dup XP_006720310.1:p.Glu382GlyfsTer8
XM_006720247.4:c.1144dup XP_006720310.1:p.Glu382GlyfsTer8
XM_011537132.1:c.1141dup XP_011535434.1:p.Glu381GlyfsTer8
XM_017021624.2:c.1141dup XP_016877113.1:p.Glu381GlyfsTer21
XM_017021625.1:c.1150dup XP_016877114.1:p.Glu384GlyfsTer21
XR_001750539.2:n.1091dup