Canonical Allele Identifier: CA390932378

Gene: VRK1

Linked Data

• MyVariant Identifiers: chr14:g.97342380A>T (hg19) ; chr14:g.96876043A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.96876043A>T , CM000676.2:g.96876043A>T	GRCh38
NC_000014.8:g.97342380A>T , CM000676.1:g.97342380A>T	GRCh37
NC_000014.7:g.96412133A>T	NCBI36
NG_016293.1:g.83697A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216639.8:c.1082A>T MANE Select	ENSP00000216639.3:p.Glu361Val
ENST00000553683.2:c.1082A>T	ENSP00000451412.2:p.Glu361Val
ENST00000555067.2:n.11136A>T
ENST00000679365.1:c.1073A>T	ENSP00000505882.1:p.Glu358Val
ENST00000679462.1:c.1117A>T	ENSP00000506011.1:p.Lys373Ter
ENST00000679506.1:n.3141A>T
ENST00000679533.1:c.*855A>T	ENSP00000505873.1:n.*855A>T
ENST00000679650.1:c.*771A>T	ENSP00000505156.1:n.*771A>T
ENST00000679727.1:c.1076A>T	ENSP00000505844.1:p.Glu359Val
ENST00000679758.1:c.1068+15308A>T	ENSP00000505539.1:n.1068+15308A>T
ENST00000679770.1:c.1082A>T	ENSP00000505214.1:p.Glu361Val
ENST00000679816.1:c.1082A>T	ENSP00000506525.1:p.Glu361Val
ENST00000679843.1:c.385A>T	ENSP00000506467.1:n.385A>T
ENST00000679903.1:c.1073A>T	ENSP00000506022.1:p.Glu358Val
ENST00000679918.1:c.1082A>T	ENSP00000505439.1:p.Glu361Val
ENST00000679941.1:c.1068+15308A>T	ENSP00000506520.1:n.1068+15308A>T
ENST00000679977.1:c.*328A>T	ENSP00000504897.1:n.*328A>T
ENST00000680007.1:c.1082A>T	ENSP00000505683.1:p.Glu361Val
ENST00000680335.1:c.1068+15308A>T	ENSP00000505806.1:n.1068+15308A>T
ENST00000680387.1:c.1079A>T	ENSP00000504908.1:p.Glu360Val
ENST00000680526.1:c.*587+15379A>T	ENSP00000505595.1:n.*587+15379A>T
ENST00000680538.1:c.992A>T	ENSP00000505611.1:p.Glu331Val
ENST00000680683.1:c.1082A>T	ENSP00000506334.1:p.Glu361Val
ENST00000680724.1:c.1082A>T	ENSP00000504891.1:p.Glu361Val
ENST00000680756.1:c.1082A>T	ENSP00000506648.1:p.Glu361Val
ENST00000680849.1:c.1079A>T	ENSP00000505602.1:p.Glu360Val
ENST00000680851.1:c.1069-5134A>T	ENSP00000505159.1:n.1069-5134A>T
ENST00000680922.1:c.*212+15308A>T	ENSP00000506480.1:n.*212+15308A>T
ENST00000680993.1:c.*432+15308A>T	ENSP00000505511.1:n.*432+15308A>T
ENST00000681061.1:c.692+15308A>T
ENST00000681101.1:c.1082A>T	ENSP00000506564.1:p.Glu361Val
ENST00000681195.1:c.1079A>T	ENSP00000504933.1:p.Glu360Val
ENST00000681249.1:c.1079A>T	ENSP00000506013.1:p.Glu360Val
ENST00000681344.1:c.1082A>T	ENSP00000506151.1:p.Glu361Val
ENST00000681355.1:c.1082A>T	ENSP00000506214.1:p.Glu361Val
ENST00000681363.1:c.*182A>T	ENSP00000505564.1:n.*182A>T
ENST00000681419.1:c.1082A>T	ENSP00000505512.1:p.Glu361Val
ENST00000681474.1:c.903A>T	ENSP00000505569.1:p.Arg301Ser
ENST00000681493.1:c.1076A>T	ENSP00000506429.1:p.Glu359Val
ENST00000681524.1:c.*226A>T	ENSP00000505783.1:n.*226A>T
ENST00000681538.1:c.*251A>T	ENSP00000506662.1:n.*251A>T
ENST00000681598.1:c.*537+15308A>T	ENSP00000506128.1:n.*537+15308A>T
ENST00000681677.1:c.706A>T
ENST00000681695.1:c.*672A>T	ENSP00000506225.1:n.*672A>T
ENST00000681778.1:c.1068+15308A>T	ENSP00000506049.1:n.1068+15308A>T
ENST00000216639.7:c.1082A>T	ENSP00000216639.3:p.Glu361Val
ENST00000553683.1:c.15A>T
ENST00000555067.1:n.312A>T
ENST00000557222.5:c.637+15308A>T
NM_003384.2:c.1082A>T	NP_003375.1:p.Glu361Val
XM_006720247.2:c.1082A>T	XP_006720310.1:p.Glu361Val
XM_011537132.1:c.1079A>T	XP_011535434.1:p.Glu360Val
XM_006720247.4:c.1082A>T	XP_006720310.1:p.Glu361Val
XM_017021624.2:c.1079A>T	XP_016877113.1:p.Glu360Val
XM_017021625.1:c.1088A>T	XP_016877114.1:p.Glu363Val
XR_001750539.2:n.1029A>T
NM_003384.3:c.1082A>T MANE Select	NP_003375.1:p.Glu361Val