Canonical Allele Identifier: CA412552195
Gene: CNKSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.21432697G>A , CM000685.2:g.21432697G>A GRCh38
NC_000023.10:g.21450815G>A , CM000685.1:g.21450815G>A GRCh37
NC_000023.9:g.21360736G>A NCBI36
NG_016266.1:g.63280G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000279451.9:c.314G>A ENSP00000279451.5:p.Gly105Glu
ENST00000379510.5:c.314G>A MANE Select ENSP00000368824.3:p.Gly105Glu
ENST00000425654.7:c.314G>A ENSP00000397906.2:p.Gly105Glu
ENST00000479158.2:n.167G>A
ENST00000480138.2:n.135G>A
ENST00000485012.2:n.412G>A
ENST00000543067.6:c.314G>A ENSP00000444633.1:p.Gly105Glu
ENST00000642359.1:c.314G>A ENSP00000496709.1:p.Gly105Glu
ENST00000642460.1:n.459G>A
ENST00000642501.1:c.-371G>A ENSP00000495189.1:n.-371G>A
ENST00000642565.1:n.483G>A
ENST00000643171.1:c.314G>A ENSP00000496186.1:p.Gly105Glu
ENST00000643220.1:c.314G>A ENSP00000495012.1:p.Gly105Glu
ENST00000643841.1:c.314G>A ENSP00000494416.1:p.Gly105Glu
ENST00000644095.1:c.314G>A ENSP00000496088.1:p.Gly105Glu
ENST00000644295.1:c.314G>A ENSP00000495501.1:p.Gly105Glu
ENST00000644585.1:c.314G>A ENSP00000495954.1:p.Gly105Glu
ENST00000644789.1:n.3452G>A
ENST00000644798.1:c.314G>A ENSP00000494983.1:p.Gly105Glu
ENST00000644832.1:n.790G>A
ENST00000645038.1:n.828G>A
ENST00000645074.1:c.314G>A ENSP00000496573.1:p.Gly105Glu
ENST00000645245.1:c.314G>A ENSP00000495695.1:p.Gly105Glu
ENST00000645791.1:c.314G>A ENSP00000494906.1:p.Gly105Glu
ENST00000646175.1:n.744G>A
ENST00000646697.1:c.250G>A
ENST00000647423.1:n.379G>A
ENST00000647532.1:n.384G>A
ENST00000279451.8:c.314G>A ENSP00000279451.4:p.Gly105Glu
ENST00000379510.3:c.314G>A ENSP00000368824.3:p.Gly105Glu
ENST00000425654.6:c.314G>A ENSP00000397906.2:p.Gly105Glu
ENST00000480138.1:n.61G>A
ENST00000543067.5:c.314G>A ENSP00000444633.1:p.Gly105Glu
NM_001168647.1:c.314G>A NP_001162118.1:p.Gly105Glu
NM_001168648.1:c.314G>A NP_001162119.1:p.Gly105Glu
NM_001168649.1:c.314G>A NP_001162120.1:p.Gly105Glu
NM_014927.3:c.314G>A NP_055742.2:p.Gly105Glu
XM_011545471.1:c.314G>A XP_011543773.1:p.Gly105Glu
XM_011545472.1:c.314G>A XP_011543774.1:p.Gly105Glu
NM_001168647.2:c.314G>A NP_001162118.1:p.Gly105Glu
NM_001168648.2:c.314G>A NP_001162119.1:p.Gly105Glu
NM_001168649.2:c.314G>A NP_001162120.1:p.Gly105Glu
NM_001330770.1:c.314G>A NP_001317699.1:p.Gly105Glu
NM_001330771.1:c.314G>A NP_001317700.1:p.Gly105Glu
NM_001330772.1:c.314G>A NP_001317701.1:p.Gly105Glu
NM_001330773.1:c.314G>A NP_001317702.1:p.Gly105Glu
NM_014927.4:c.314G>A NP_055742.2:p.Gly105Glu
XM_011545471.3:c.314G>A XP_011543773.1:p.Gly105Glu
XM_011545472.3:c.314G>A XP_011543774.1:p.Gly105Glu
XM_017029358.2:c.314G>A XP_016884847.1:p.Gly105Glu
NM_014927.5:c.314G>A MANE Select NP_055742.2:p.Gly105Glu
NM_001168647.3:c.314G>A NP_001162118.1:p.Gly105Glu
NM_001168648.3:c.314G>A NP_001162119.1:p.Gly105Glu
NM_001168649.3:c.314G>A NP_001162120.1:p.Gly105Glu
NM_001330770.2:c.314G>A NP_001317699.1:p.Gly105Glu
NM_001330771.2:c.314G>A NP_001317700.1:p.Gly105Glu
NM_001330772.2:c.314G>A NP_001317701.1:p.Gly105Glu
NM_001330773.2:c.314G>A NP_001317702.1:p.Gly105Glu