Canonical Allele Identifier: CA2693293207

Gene: CNKSR2

Linked Data

• gnomAD v4: X-21606905-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.21606905T>G , CM000685.2:g.21606905T>G	GRCh38
NC_000023.10:g.21625023T>G , CM000685.1:g.21625023T>G	GRCh37
NC_000023.9:g.21534944T>G	NCBI36
NG_016266.1:g.237488T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000279451.9:c.2055+26T>G	ENSP00000279451.5:n.2055+26T>G
ENST00000379510.5:c.2145+26T>G MANE Select	ENSP00000368824.3:n.2145+26T>G
ENST00000425654.7:c.2055+26T>G	ENSP00000397906.2:n.2055+26T>G
ENST00000543067.6:c.1998+26T>G	ENSP00000444633.1:n.1998+26T>G
ENST00000642359.1:c.2145+26T>G	ENSP00000496709.1:n.2145+26T>G
ENST00000642501.1:c.1224+26T>G	ENSP00000495189.1:n.1224+26T>G
ENST00000642853.1:n.1923+26T>G
ENST00000643156.1:c.977+26T>G
ENST00000643171.1:c.1998+26T>G	ENSP00000496186.1:n.1998+26T>G
ENST00000643220.1:c.1896+26T>G	ENSP00000495012.1:n.1896+26T>G
ENST00000643313.1:c.1297+26T>G
ENST00000644075.1:n.1511+26T>G
ENST00000644095.1:c.1998+26T>G	ENSP00000496088.1:n.1998+26T>G
ENST00000644295.1:c.2070+26T>G	ENSP00000495501.1:n.2070+26T>G
ENST00000644585.1:c.1998+26T>G	ENSP00000495954.1:n.1998+26T>G
ENST00000645074.1:c.1494+26T>G	ENSP00000496573.1:n.1494+26T>G
ENST00000645245.1:c.1908+26T>G	ENSP00000495695.1:n.1908+26T>G
ENST00000645539.1:n.342+26T>G
ENST00000645791.1:c.1908+26T>G	ENSP00000494906.1:n.1908+26T>G
ENST00000646690.1:n.153+26T>G
ENST00000646697.1:c.2161+26T>G
ENST00000647058.1:n.694+26T>G
ENST00000647349.1:n.1449+26T>G
ENST00000647532.1:n.5904+26T>G
ENST00000279451.8:c.2145+26T>G	ENSP00000279451.4:n.2145+26T>G
ENST00000379510.3:c.2145+26T>G	ENSP00000368824.3:n.2145+26T>G
ENST00000425654.6:c.2055+26T>G	ENSP00000397906.2:n.2055+26T>G
ENST00000543067.5:c.1998+26T>G	ENSP00000444633.1:n.1998+26T>G
NM_001168647.1:c.2055+26T>G	NP_001162118.1:n.2055+26T>G
NM_001168648.1:c.2145+26T>G	NP_001162119.1:n.2145+26T>G
NM_001168649.1:c.1998+26T>G	NP_001162120.1:n.1998+26T>G
NM_014927.3:c.2145+26T>G	NP_055742.2:n.2145+26T>G
XM_011545471.1:c.2055+26T>G	XP_011543773.1:n.2055+26T>G
XM_011545472.1:c.1998+26T>G	XP_011543774.1:n.1998+26T>G
NM_001168647.2:c.2055+26T>G	NP_001162118.1:n.2055+26T>G
NM_001168648.2:c.2145+26T>G	NP_001162119.1:n.2145+26T>G
NM_001168649.2:c.1998+26T>G	NP_001162120.1:n.1998+26T>G
NM_001330770.1:c.1998+26T>G	NP_001317699.1:n.1998+26T>G
NM_001330771.1:c.1908+26T>G	NP_001317700.1:n.1908+26T>G
NM_001330772.1:c.1908+26T>G	NP_001317701.1:n.1908+26T>G
NM_001330773.1:c.2055+26T>G	NP_001317702.1:n.2055+26T>G
NM_014927.4:c.2145+26T>G	NP_055742.2:n.2145+26T>G
XM_011545471.3:c.2055+26T>G	XP_011543773.1:n.2055+26T>G
XM_011545472.3:c.1998+26T>G	XP_011543774.1:n.1998+26T>G
XM_017029358.2:c.1908+26T>G	XP_016884847.1:n.1908+26T>G
NM_014927.5:c.2145+26T>G MANE Select	NP_055742.2:n.2145+26T>G
NM_001168647.3:c.2055+26T>G	NP_001162118.1:n.2055+26T>G
NM_001168648.3:c.2145+26T>G	NP_001162119.1:n.2145+26T>G
NM_001168649.3:c.1998+26T>G	NP_001162120.1:n.1998+26T>G
NM_001330770.2:c.1998+26T>G	NP_001317699.1:n.1998+26T>G
NM_001330771.2:c.1908+26T>G	NP_001317700.1:n.1908+26T>G
NM_001330772.2:c.1908+26T>G	NP_001317701.1:n.1908+26T>G
NM_001330773.2:c.2055+26T>G	NP_001317702.1:n.2055+26T>G