Canonical Allele Identifier: CA10366541

Gene: CNKSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.21516570G>A , CM000685.2:g.21516570G>A	GRCh38
NC_000023.10:g.21534688G>A , CM000685.1:g.21534688G>A	GRCh37
NC_000023.9:g.21444609G>A	NCBI36
NG_016266.1:g.147153G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279451.9:c.896G>A	ENSP00000279451.5:p.Ser299Asn
ENST00000379510.5:c.896G>A MANE Select	ENSP00000368824.3:p.Ser299Asn
ENST00000425654.7:c.896G>A	ENSP00000397906.2:p.Ser299Asn
ENST00000479158.2:n.663+14982G>A
ENST00000485012.2:n.909-10297G>A
ENST00000543067.6:c.811-10297G>A	ENSP00000444633.1:n.811-10297G>A
ENST00000642359.1:c.896G>A	ENSP00000496709.1:p.Ser299Asn
ENST00000642460.1:n.956-10297G>A
ENST00000642501.1:c.127-10297G>A	ENSP00000495189.1:n.127-10297G>A
ENST00000643171.1:c.811-10297G>A	ENSP00000496186.1:n.811-10297G>A
ENST00000643220.1:c.811-10297G>A	ENSP00000495012.1:n.811-10297G>A
ENST00000643313.1:c.138G>A
ENST00000644075.1:n.324-10297G>A
ENST00000644095.1:c.811-10297G>A	ENSP00000496088.1:n.811-10297G>A
ENST00000644295.1:c.811-10297G>A	ENSP00000495501.1:n.811-10297G>A
ENST00000644585.1:c.811-10297G>A	ENSP00000495954.1:n.811-10297G>A
ENST00000644789.1:n.4034G>A
ENST00000645038.1:n.1410G>A
ENST00000645074.1:c.896G>A	ENSP00000496573.1:p.Ser299Asn
ENST00000645245.1:c.811-10297G>A	ENSP00000495695.1:n.811-10297G>A
ENST00000645791.1:c.811-10297G>A	ENSP00000494906.1:n.811-10297G>A
ENST00000646697.1:c.912G>A
ENST00000647349.1:n.200G>A
ENST00000647423.1:n.961G>A
ENST00000647532.1:n.966G>A
ENST00000279451.8:c.896G>A	ENSP00000279451.4:p.Ser299Asn
ENST00000379510.3:c.896G>A	ENSP00000368824.3:p.Ser299Asn
ENST00000425654.6:c.896G>A	ENSP00000397906.2:p.Ser299Asn
ENST00000479158.1:n.250-10297G>A
ENST00000543067.5:c.811-10297G>A	ENSP00000444633.1:n.811-10297G>A
NM_001168647.1:c.896G>A	NP_001162118.1:p.Ser299Asn
NM_001168648.1:c.896G>A	NP_001162119.1:p.Ser299Asn
NM_001168649.1:c.811-10297G>A	NP_001162120.1:n.811-10297G>A
NM_014927.3:c.896G>A	NP_055742.2:p.Ser299Asn
XM_011545471.1:c.896G>A	XP_011543773.1:p.Ser299Asn
XM_011545472.1:c.811-10297G>A	XP_011543774.1:n.811-10297G>A
NM_001168647.2:c.896G>A	NP_001162118.1:p.Ser299Asn
NM_001168648.2:c.896G>A	NP_001162119.1:p.Ser299Asn
NM_001168649.2:c.811-10297G>A	NP_001162120.1:n.811-10297G>A
NM_001330770.1:c.811-10297G>A	NP_001317699.1:n.811-10297G>A
NM_001330771.1:c.811-10297G>A	NP_001317700.1:n.811-10297G>A
NM_001330772.1:c.811-10297G>A	NP_001317701.1:n.811-10297G>A
NM_001330773.1:c.896G>A	NP_001317702.1:p.Ser299Asn
NM_014927.4:c.896G>A	NP_055742.2:p.Ser299Asn
XM_011545471.3:c.896G>A	XP_011543773.1:p.Ser299Asn
XM_011545472.3:c.811-10297G>A	XP_011543774.1:n.811-10297G>A
XM_017029358.2:c.811-10297G>A	XP_016884847.1:n.811-10297G>A
NM_014927.5:c.896G>A MANE Select	NP_055742.2:p.Ser299Asn
NM_001168647.3:c.896G>A	NP_001162118.1:p.Ser299Asn
NM_001168648.3:c.896G>A	NP_001162119.1:p.Ser299Asn
NM_001168649.3:c.811-10297G>A	NP_001162120.1:n.811-10297G>A
NM_001330770.2:c.811-10297G>A	NP_001317699.1:n.811-10297G>A
NM_001330771.2:c.811-10297G>A	NP_001317700.1:n.811-10297G>A
NM_001330772.2:c.811-10297G>A	NP_001317701.1:n.811-10297G>A
NM_001330773.2:c.896G>A	NP_001317702.1:p.Ser299Asn