Canonical Allele Identifier: CA412556664

Gene: CNKSR2

Linked Data

• gnomAD v4: X-21606787-A-G
• MyVariant Identifiers: chrX:g.21624905A>G (hg19) ; chrX:g.21606787A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.21606787A>G , CM000685.2:g.21606787A>G	GRCh38
NC_000023.10:g.21624905A>G , CM000685.1:g.21624905A>G	GRCh37
NC_000023.9:g.21534826A>G	NCBI36
NG_016266.1:g.237370A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000279451.9:c.1963A>G	ENSP00000279451.5:p.Ser655Gly
ENST00000379510.5:c.2053A>G MANE Select	ENSP00000368824.3:p.Ser685Gly
ENST00000425654.7:c.1963A>G	ENSP00000397906.2:p.Ser655Gly
ENST00000543067.6:c.1906A>G	ENSP00000444633.1:p.Ser636Gly
ENST00000642359.1:c.2053A>G	ENSP00000496709.1:p.Ser685Gly
ENST00000642501.1:c.1132A>G	ENSP00000495189.1:p.Ser378Gly
ENST00000642853.1:n.1831A>G
ENST00000643156.1:c.885A>G
ENST00000643171.1:c.1906A>G	ENSP00000496186.1:p.Ser636Gly
ENST00000643220.1:c.1804A>G	ENSP00000495012.1:p.Ser602Gly
ENST00000643313.1:c.1205A>G
ENST00000644075.1:n.1419A>G
ENST00000644095.1:c.1906A>G	ENSP00000496088.1:p.Ser636Gly
ENST00000644295.1:c.1978A>G	ENSP00000495501.1:p.Ser660Gly
ENST00000644585.1:c.1906A>G	ENSP00000495954.1:p.Ser636Gly
ENST00000645074.1:c.1402A>G	ENSP00000496573.1:p.Ser468Gly
ENST00000645245.1:c.1816A>G	ENSP00000495695.1:p.Ser606Gly
ENST00000645539.1:n.250A>G
ENST00000645791.1:c.1816A>G	ENSP00000494906.1:p.Ser606Gly
ENST00000646690.1:n.61A>G
ENST00000646697.1:c.2069A>G
ENST00000647058.1:n.602A>G
ENST00000647349.1:n.1357A>G
ENST00000647532.1:n.5812A>G
ENST00000279451.8:c.2053A>G	ENSP00000279451.4:p.Ser685Gly
ENST00000379510.3:c.2053A>G	ENSP00000368824.3:p.Ser685Gly
ENST00000425654.6:c.1963A>G	ENSP00000397906.2:p.Ser655Gly
ENST00000543067.5:c.1906A>G	ENSP00000444633.1:p.Ser636Gly
NM_001168647.1:c.1963A>G	NP_001162118.1:p.Ser655Gly
NM_001168648.1:c.2053A>G	NP_001162119.1:p.Ser685Gly
NM_001168649.1:c.1906A>G	NP_001162120.1:p.Ser636Gly
NM_014927.3:c.2053A>G	NP_055742.2:p.Ser685Gly
XM_011545471.1:c.1963A>G	XP_011543773.1:p.Ser655Gly
XM_011545472.1:c.1906A>G	XP_011543774.1:p.Ser636Gly
NM_001168647.2:c.1963A>G	NP_001162118.1:p.Ser655Gly
NM_001168648.2:c.2053A>G	NP_001162119.1:p.Ser685Gly
NM_001168649.2:c.1906A>G	NP_001162120.1:p.Ser636Gly
NM_001330770.1:c.1906A>G	NP_001317699.1:p.Ser636Gly
NM_001330771.1:c.1816A>G	NP_001317700.1:p.Ser606Gly
NM_001330772.1:c.1816A>G	NP_001317701.1:p.Ser606Gly
NM_001330773.1:c.1963A>G	NP_001317702.1:p.Ser655Gly
NM_014927.4:c.2053A>G	NP_055742.2:p.Ser685Gly
XM_011545471.3:c.1963A>G	XP_011543773.1:p.Ser655Gly
XM_011545472.3:c.1906A>G	XP_011543774.1:p.Ser636Gly
XM_017029358.2:c.1816A>G	XP_016884847.1:p.Ser606Gly
NM_014927.5:c.2053A>G MANE Select	NP_055742.2:p.Ser685Gly
NM_001168647.3:c.1963A>G	NP_001162118.1:p.Ser655Gly
NM_001168648.3:c.2053A>G	NP_001162119.1:p.Ser685Gly
NM_001168649.3:c.1906A>G	NP_001162120.1:p.Ser636Gly
NM_001330770.2:c.1906A>G	NP_001317699.1:p.Ser636Gly
NM_001330771.2:c.1816A>G	NP_001317700.1:p.Ser606Gly
NM_001330772.2:c.1816A>G	NP_001317701.1:p.Ser606Gly
NM_001330773.2:c.1963A>G	NP_001317702.1:p.Ser655Gly