Canonical Allele Identifier: CA645601267

Gene: CNKSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.21595045dup , CM000685.2:g.21595045dup	GRCh38
NC_000023.10:g.21613163dup , CM000685.1:g.21613163dup	GRCh37
NC_000023.9:g.21523084dup	NCBI36
NG_016266.1:g.225628dup

Transcript Alleles

HGVS	Amino-acid Change
NM_014927.5:c.1902dup MANE Select	NP_055742.2:p.Tyr635IlefsTer9
ENST00000379510.5:c.1902dup MANE Select	ENSP00000368824.3:p.Tyr635IlefsTer9
NM_001168647.1:c.1812dup	NP_001162118.1:p.Tyr605IlefsTer9
NM_001168647.2:c.1812dup	NP_001162118.1:p.Tyr605IlefsTer9
NM_001168647.3:c.1812dup	NP_001162118.1:p.Tyr605IlefsTer9
NM_001168648.1:c.1902dup	NP_001162119.1:p.Tyr635IlefsTer9
NM_001168648.2:c.1902dup	NP_001162119.1:p.Tyr635IlefsTer9
NM_001168648.3:c.1902dup	NP_001162119.1:p.Tyr635IlefsTer9
NM_001168649.1:c.1755dup	NP_001162120.1:p.Tyr586IlefsTer9
NM_001168649.2:c.1755dup	NP_001162120.1:p.Tyr586IlefsTer9
NM_001168649.3:c.1755dup	NP_001162120.1:p.Tyr586IlefsTer9
NM_001330770.1:c.1755dup	NP_001317699.1:p.Tyr586IlefsTer9
NM_001330770.2:c.1755dup	NP_001317699.1:p.Tyr586IlefsTer9
NM_001330771.1:c.1665dup	NP_001317700.1:p.Tyr556IlefsTer9
NM_001330771.2:c.1665dup	NP_001317700.1:p.Tyr556IlefsTer9
NM_001330772.1:c.1665dup	NP_001317701.1:p.Tyr556IlefsTer9
NM_001330772.2:c.1665dup	NP_001317701.1:p.Tyr556IlefsTer9
NM_001330773.1:c.1812dup	NP_001317702.1:p.Tyr605IlefsTer9
NM_001330773.2:c.1812dup	NP_001317702.1:p.Tyr605IlefsTer9
NM_014927.3:c.1902dup	NP_055742.2:p.Tyr635IlefsTer9
NM_014927.4:c.1902dup	NP_055742.2:p.Tyr635IlefsTer9
ENST00000279451.8:c.1902dup	ENSP00000279451.4:p.Tyr635IlefsTer9
ENST00000279451.9:c.1812dup	ENSP00000279451.5:p.Tyr605IlefsTer9
ENST00000379510.3:c.1902dup	ENSP00000368824.3:p.Tyr635IlefsTer9
ENST00000425654.6:c.1812dup	ENSP00000397906.2:p.Tyr605IlefsTer9
ENST00000425654.7:c.1812dup	ENSP00000397906.2:p.Tyr605IlefsTer9
ENST00000543067.5:c.1755dup	ENSP00000444633.1:p.Tyr586IlefsTer9
ENST00000543067.6:c.1755dup	ENSP00000444633.1:p.Tyr586IlefsTer9
ENST00000642359.1:c.1902dup	ENSP00000496709.1:p.Tyr635IlefsTer9
ENST00000642501.1:c.981dup	ENSP00000495189.1:p.Tyr328IlefsTer9
ENST00000642853.1:n.1680dup
ENST00000643156.1:c.737-279dup
ENST00000643171.1:c.1755dup	ENSP00000496186.1:p.Tyr586IlefsTer9
ENST00000643220.1:c.1653dup	ENSP00000495012.1:p.Tyr552IlefsTer9
ENST00000643313.1:c.1054dup
ENST00000644075.1:n.1268dup
ENST00000644095.1:c.1755dup	ENSP00000496088.1:p.Tyr586IlefsTer9
ENST00000644295.1:c.1827dup	ENSP00000495501.1:p.Tyr610IlefsTer9
ENST00000644585.1:c.1755dup	ENSP00000495954.1:p.Tyr586IlefsTer9
ENST00000645074.1:c.1251dup	ENSP00000496573.1:p.Tyr418IlefsTer9
ENST00000645245.1:c.1665dup	ENSP00000495695.1:p.Tyr556IlefsTer9
ENST00000645791.1:c.1665dup	ENSP00000494906.1:p.Tyr556IlefsTer9
ENST00000646697.1:c.1918dup
ENST00000647058.1:n.175dup
ENST00000647349.1:n.1206dup
ENST00000647532.1:n.5661dup
XM_011545471.1:c.1812dup	XP_011543773.1:p.Tyr605IlefsTer9
XM_011545471.3:c.1812dup	XP_011543773.1:p.Tyr605IlefsTer9
XM_011545472.1:c.1755dup	XP_011543774.1:p.Tyr586IlefsTer9
XM_011545472.3:c.1755dup	XP_011543774.1:p.Tyr586IlefsTer9
XM_017029358.2:c.1665dup	XP_016884847.1:p.Tyr556IlefsTer9