Canonical Allele Identifier: CA390930675

Gene: VRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.96853167G>A , CM000676.2:g.96853167G>A	GRCh38
NC_000014.8:g.97319504G>A , CM000676.1:g.97319504G>A	GRCh37
NC_000014.7:g.96389257G>A	NCBI36
NG_016293.1:g.60821G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003384.3:c.576+1G>A MANE Select	NP_003375.1:n.576+1G>A
ENST00000216639.8:c.576+1G>A MANE Select	ENSP00000216639.3:n.576+1G>A
NM_003384.2:c.576+1G>A	NP_003375.1:n.576+1G>A
ENST00000216639.7:c.576+1G>A	ENSP00000216639.3:n.576+1G>A
ENST00000553683.2:c.576+1G>A	ENSP00000451412.2:n.576+1G>A
ENST00000555351.2:n.833G>A
ENST00000557222.5:c.145+1G>A
ENST00000557222.6:c.192+1G>A	ENSP00000450820.2:n.192+1G>A
ENST00000557352.2:c.576+1G>A	ENSP00000451682.2:n.576+1G>A
ENST00000679365.1:c.570+1G>A	ENSP00000505882.1:n.570+1G>A
ENST00000679452.1:c.*188+1G>A	ENSP00000505395.1:n.*188+1G>A
ENST00000679462.1:c.576+1G>A	ENSP00000506011.1:n.576+1G>A
ENST00000679506.1:n.582G>A
ENST00000679533.1:c.*349+1G>A	ENSP00000505873.1:n.*349+1G>A
ENST00000679650.1:c.*265+1G>A	ENSP00000505156.1:n.*265+1G>A
ENST00000679727.1:c.570+1G>A	ENSP00000505844.1:n.570+1G>A
ENST00000679736.1:c.576+1G>A	ENSP00000506517.1:n.576+1G>A
ENST00000679758.1:c.576+1G>A	ENSP00000505539.1:n.576+1G>A
ENST00000679770.1:c.576+1G>A	ENSP00000505214.1:n.576+1G>A
ENST00000679816.1:c.576+1G>A	ENSP00000506525.1:n.576+1G>A
ENST00000679903.1:c.576+1G>A	ENSP00000506022.1:n.576+1G>A
ENST00000679918.1:c.576+1G>A	ENSP00000505439.1:n.576+1G>A
ENST00000679941.1:c.576+1G>A	ENSP00000506520.1:n.576+1G>A
ENST00000679977.1:c.576+1G>A	ENSP00000504897.1:n.576+1G>A
ENST00000680007.1:c.576+1G>A	ENSP00000505683.1:n.576+1G>A
ENST00000680084.1:n.682+1G>A
ENST00000680222.1:c.*260+1G>A	ENSP00000506647.1:n.*260+1G>A
ENST00000680335.1:c.576+1G>A	ENSP00000505806.1:n.576+1G>A
ENST00000680339.1:c.*265+1G>A	ENSP00000506470.1:n.*265+1G>A
ENST00000680348.1:c.*61+1G>A	ENSP00000504922.1:n.*61+1G>A
ENST00000680384.1:c.*466+1G>A	ENSP00000506237.1:n.*466+1G>A
ENST00000680387.1:c.576+1G>A	ENSP00000504908.1:n.576+1G>A
ENST00000680509.1:c.576+1G>A	ENSP00000505209.1:n.576+1G>A
ENST00000680526.1:c.*166+1G>A	ENSP00000505595.1:n.*166+1G>A
ENST00000680538.1:c.576+1G>A	ENSP00000505611.1:n.576+1G>A
ENST00000680683.1:c.576+1G>A	ENSP00000506334.1:n.576+1G>A
ENST00000680724.1:c.576+1G>A	ENSP00000504891.1:n.576+1G>A
ENST00000680756.1:c.576+1G>A	ENSP00000506648.1:n.576+1G>A
ENST00000680849.1:c.573+1G>A	ENSP00000505602.1:n.573+1G>A
ENST00000680851.1:c.576+1G>A	ENSP00000505159.1:n.576+1G>A
ENST00000680922.1:c.576+1G>A	ENSP00000506480.1:n.576+1G>A
ENST00000680993.1:c.*61+1G>A	ENSP00000505511.1:n.*61+1G>A
ENST00000681061.1:c.200+1G>A
ENST00000681077.1:c.*210+1G>A	ENSP00000505642.1:n.*210+1G>A
ENST00000681101.1:c.576+1G>A	ENSP00000506564.1:n.576+1G>A
ENST00000681176.1:c.450+1G>A	ENSP00000505454.1:n.450+1G>A
ENST00000681195.1:c.576+1G>A	ENSP00000504933.1:n.576+1G>A
ENST00000681249.1:c.576+1G>A	ENSP00000506013.1:n.576+1G>A
ENST00000681344.1:c.576+1G>A	ENSP00000506151.1:n.576+1G>A
ENST00000681355.1:c.576+1G>A	ENSP00000506214.1:n.576+1G>A
ENST00000681363.1:c.576+1G>A	ENSP00000505564.1:n.576+1G>A
ENST00000681419.1:c.576+1G>A	ENSP00000505512.1:n.576+1G>A
ENST00000681474.1:c.576+1G>A	ENSP00000505569.1:n.576+1G>A
ENST00000681493.1:c.576+1G>A	ENSP00000506429.1:n.576+1G>A
ENST00000681524.1:c.576+1G>A	ENSP00000505783.1:n.576+1G>A
ENST00000681538.1:c.576+1G>A	ENSP00000506662.1:n.576+1G>A
ENST00000681598.1:c.*166+1G>A	ENSP00000506128.1:n.*166+1G>A
ENST00000681677.1:c.200+1G>A
ENST00000681695.1:c.*166+1G>A	ENSP00000506225.1:n.*166+1G>A
ENST00000681778.1:c.576+1G>A	ENSP00000506049.1:n.576+1G>A
ENST00000681785.1:c.576+1G>A	ENSP00000505166.1:n.576+1G>A
XM_006720247.2:c.576+1G>A	XP_006720310.1:n.576+1G>A
XM_006720247.4:c.576+1G>A	XP_006720310.1:n.576+1G>A
XM_011537132.1:c.576+1G>A	XP_011535434.1:n.576+1G>A
XM_017021624.2:c.576+1G>A	XP_016877113.1:n.576+1G>A
XM_017021625.1:c.582+1G>A	XP_016877114.1:n.582+1G>A
XM_017021626.2:c.576+1G>A	XP_016877115.1:n.576+1G>A
XR_001750539.2:n.644+1G>A