Canonical Allele Identifier: CA390932355

Gene: VRK1

Linked Data

• MyVariant Identifiers: chr14:g.97342371G>C (hg19) ; chr14:g.96876034G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.96876034G>C , CM000676.2:g.96876034G>C	GRCh38
NC_000014.8:g.97342371G>C , CM000676.1:g.97342371G>C	GRCh37
NC_000014.7:g.96412124G>C	NCBI36
NG_016293.1:g.83688G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000216639.8:c.1073G>C MANE Select	ENSP00000216639.3:p.Arg358Pro
ENST00000553683.2:c.1073G>C	ENSP00000451412.2:p.Arg358Pro
ENST00000555067.2:n.11127G>C
ENST00000679365.1:c.1064G>C	ENSP00000505882.1:p.Arg355Pro
ENST00000679462.1:c.1108G>C	ENSP00000506011.1:p.Glu370Gln
ENST00000679506.1:n.3132G>C
ENST00000679533.1:c.*846G>C	ENSP00000505873.1:n.*846G>C
ENST00000679650.1:c.*762G>C	ENSP00000505156.1:n.*762G>C
ENST00000679727.1:c.1067G>C	ENSP00000505844.1:p.Arg356Pro
ENST00000679758.1:c.1068+15299G>C	ENSP00000505539.1:n.1068+15299G>C
ENST00000679770.1:c.1073G>C	ENSP00000505214.1:p.Arg358Pro
ENST00000679816.1:c.1073G>C	ENSP00000506525.1:p.Arg358Pro
ENST00000679843.1:c.376G>C	ENSP00000506467.1:n.376G>C
ENST00000679903.1:c.1069-5G>C	ENSP00000506022.1:n.1069-5G>C
ENST00000679918.1:c.1073G>C	ENSP00000505439.1:p.Arg358Pro
ENST00000679941.1:c.1068+15299G>C	ENSP00000506520.1:n.1068+15299G>C
ENST00000679977.1:c.*319G>C	ENSP00000504897.1:n.*319G>C
ENST00000680007.1:c.1073G>C	ENSP00000505683.1:p.Arg358Pro
ENST00000680335.1:c.1068+15299G>C	ENSP00000505806.1:n.1068+15299G>C
ENST00000680387.1:c.1070G>C	ENSP00000504908.1:p.Arg357Pro
ENST00000680526.1:c.*587+15370G>C	ENSP00000505595.1:n.*587+15370G>C
ENST00000680538.1:c.983G>C	ENSP00000505611.1:p.Arg328Pro
ENST00000680683.1:c.1073G>C	ENSP00000506334.1:p.Arg358Pro
ENST00000680724.1:c.1073G>C	ENSP00000504891.1:p.Arg358Pro
ENST00000680756.1:c.1073G>C	ENSP00000506648.1:p.Arg358Pro
ENST00000680849.1:c.1070G>C	ENSP00000505602.1:p.Arg357Pro
ENST00000680851.1:c.1069-5143G>C	ENSP00000505159.1:n.1069-5143G>C
ENST00000680922.1:c.*212+15299G>C	ENSP00000506480.1:n.*212+15299G>C
ENST00000680993.1:c.*432+15299G>C	ENSP00000505511.1:n.*432+15299G>C
ENST00000681061.1:c.692+15299G>C
ENST00000681101.1:c.1073G>C	ENSP00000506564.1:p.Arg358Pro
ENST00000681195.1:c.1070G>C	ENSP00000504933.1:p.Arg357Pro
ENST00000681249.1:c.1070G>C	ENSP00000506013.1:p.Arg357Pro
ENST00000681344.1:c.1073G>C	ENSP00000506151.1:p.Arg358Pro
ENST00000681355.1:c.1073G>C	ENSP00000506214.1:p.Arg358Pro
ENST00000681363.1:c.*173G>C	ENSP00000505564.1:n.*173G>C
ENST00000681419.1:c.1073G>C	ENSP00000505512.1:p.Arg358Pro
ENST00000681474.1:c.894G>C	ENSP00000505569.1:p.Ala298=
ENST00000681493.1:c.1067G>C	ENSP00000506429.1:p.Arg356Pro
ENST00000681524.1:c.*217G>C	ENSP00000505783.1:n.*217G>C
ENST00000681538.1:c.*242G>C	ENSP00000506662.1:n.*242G>C
ENST00000681598.1:c.*537+15299G>C	ENSP00000506128.1:n.*537+15299G>C
ENST00000681677.1:c.697G>C
ENST00000681695.1:c.*663G>C	ENSP00000506225.1:n.*663G>C
ENST00000681778.1:c.1068+15299G>C	ENSP00000506049.1:n.1068+15299G>C
ENST00000216639.7:c.1073G>C	ENSP00000216639.3:p.Arg358Pro
ENST00000553683.1:c.6G>C
ENST00000555067.1:n.303G>C
ENST00000557222.5:c.637+15299G>C
NM_003384.2:c.1073G>C	NP_003375.1:p.Arg358Pro
XM_006720247.2:c.1073G>C	XP_006720310.1:p.Arg358Pro
XM_011537132.1:c.1070G>C	XP_011535434.1:p.Arg357Pro
XM_006720247.4:c.1073G>C	XP_006720310.1:p.Arg358Pro
XM_017021624.2:c.1070G>C	XP_016877113.1:p.Arg357Pro
XM_017021625.1:c.1079G>C	XP_016877114.1:p.Arg360Pro
XR_001750539.2:n.1020G>C
NM_003384.3:c.1073G>C MANE Select	NP_003375.1:p.Arg358Pro