Canonical Allele Identifier: CA412558611

Gene: CNKSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.21609261C>G , CM000685.2:g.21609261C>G	GRCh38
NC_000023.10:g.21627379C>G , CM000685.1:g.21627379C>G	GRCh37
NC_000023.9:g.21537300C>G	NCBI36
NG_016266.1:g.239844C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279451.9:c.2246C>G	ENSP00000279451.5:p.Ser749Ter
ENST00000379510.5:c.2336C>G MANE Select	ENSP00000368824.3:p.Ser779Ter
ENST00000425654.7:c.2246C>G	ENSP00000397906.2:p.Ser749Ter
ENST00000543067.6:c.2189C>G	ENSP00000444633.1:p.Ser730Ter
ENST00000642359.1:c.2336C>G	ENSP00000496709.1:p.Ser779Ter
ENST00000642501.1:c.1415C>G	ENSP00000495189.1:p.Ser472Ter
ENST00000642853.1:n.2114C>G
ENST00000643156.1:c.1168C>G
ENST00000643171.1:c.*283C>G	ENSP00000496186.1:n.*283C>G
ENST00000643220.1:c.2087C>G	ENSP00000495012.1:p.Ser696Ter
ENST00000643313.1:c.1488C>G
ENST00000644075.1:n.1702C>G
ENST00000644095.1:c.2189C>G	ENSP00000496088.1:p.Ser730Ter
ENST00000644295.1:c.2261C>G	ENSP00000495501.1:p.Ser754Ter
ENST00000644585.1:c.2189C>G	ENSP00000495954.1:p.Ser730Ter
ENST00000645074.1:c.1685C>G	ENSP00000496573.1:p.Ser562Ter
ENST00000645245.1:c.2099C>G	ENSP00000495695.1:p.Ser700Ter
ENST00000645539.1:n.533C>G
ENST00000645791.1:c.2099C>G	ENSP00000494906.1:p.Ser700Ter
ENST00000646690.1:n.344C>G
ENST00000646697.1:c.2352C>G
ENST00000647058.1:n.885C>G
ENST00000647349.1:n.1640C>G
ENST00000647532.1:n.6095C>G
ENST00000279451.8:c.2336C>G	ENSP00000279451.4:p.Ser779Ter
ENST00000379510.3:c.2336C>G	ENSP00000368824.3:p.Ser779Ter
ENST00000425654.6:c.2246C>G	ENSP00000397906.2:p.Ser749Ter
ENST00000543067.5:c.2189C>G	ENSP00000444633.1:p.Ser730Ter
NM_001168647.1:c.2246C>G	NP_001162118.1:p.Ser749Ter
NM_001168648.1:c.2336C>G	NP_001162119.1:p.Ser779Ter
NM_001168649.1:c.2189C>G	NP_001162120.1:p.Ser730Ter
NM_014927.3:c.2336C>G	NP_055742.2:p.Ser779Ter
XM_011545471.1:c.2246C>G	XP_011543773.1:p.Ser749Ter
XM_011545472.1:c.2189C>G	XP_011543774.1:p.Ser730Ter
NM_001168647.2:c.2246C>G	NP_001162118.1:p.Ser749Ter
NM_001168648.2:c.2336C>G	NP_001162119.1:p.Ser779Ter
NM_001168649.2:c.2189C>G	NP_001162120.1:p.Ser730Ter
NM_001330770.1:c.2189C>G	NP_001317699.1:p.Ser730Ter
NM_001330771.1:c.2099C>G	NP_001317700.1:p.Ser700Ter
NM_001330772.1:c.2099C>G	NP_001317701.1:p.Ser700Ter
NM_001330773.1:c.2246C>G	NP_001317702.1:p.Ser749Ter
NM_014927.4:c.2336C>G	NP_055742.2:p.Ser779Ter
XM_011545471.3:c.2246C>G	XP_011543773.1:p.Ser749Ter
XM_011545472.3:c.2189C>G	XP_011543774.1:p.Ser730Ter
XM_017029358.2:c.2099C>G	XP_016884847.1:p.Ser700Ter
NM_014927.5:c.2336C>G MANE Select	NP_055742.2:p.Ser779Ter
NM_001168647.3:c.2246C>G	NP_001162118.1:p.Ser749Ter
NM_001168648.3:c.2336C>G	NP_001162119.1:p.Ser779Ter
NM_001168649.3:c.2189C>G	NP_001162120.1:p.Ser730Ter
NM_001330770.2:c.2189C>G	NP_001317699.1:p.Ser730Ter
NM_001330771.2:c.2099C>G	NP_001317700.1:p.Ser700Ter
NM_001330772.2:c.2099C>G	NP_001317701.1:p.Ser700Ter
NM_001330773.2:c.2246C>G	NP_001317702.1:p.Ser749Ter