Canonical Allele Identifier: CA412556659

Gene: CNKSR2

Linked Data

• MyVariant Identifiers: chrX:g.21624903G>C (hg19) ; chrX:g.21606785G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.21606785G>C , CM000685.2:g.21606785G>C	GRCh38
NC_000023.10:g.21624903G>C , CM000685.1:g.21624903G>C	GRCh37
NC_000023.9:g.21534824G>C	NCBI36
NG_016266.1:g.237368G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000279451.9:c.1961G>C	ENSP00000279451.5:p.Trp654Ser
ENST00000379510.5:c.2051G>C MANE Select	ENSP00000368824.3:p.Trp684Ser
ENST00000425654.7:c.1961G>C	ENSP00000397906.2:p.Trp654Ser
ENST00000543067.6:c.1904G>C	ENSP00000444633.1:p.Trp635Ser
ENST00000642359.1:c.2051G>C	ENSP00000496709.1:p.Trp684Ser
ENST00000642501.1:c.1130G>C	ENSP00000495189.1:p.Trp377Ser
ENST00000642853.1:n.1829G>C
ENST00000643156.1:c.883G>C
ENST00000643171.1:c.1904G>C	ENSP00000496186.1:p.Trp635Ser
ENST00000643220.1:c.1802G>C	ENSP00000495012.1:p.Trp601Ser
ENST00000643313.1:c.1203G>C
ENST00000644075.1:n.1417G>C
ENST00000644095.1:c.1904G>C	ENSP00000496088.1:p.Trp635Ser
ENST00000644295.1:c.1976G>C	ENSP00000495501.1:p.Trp659Ser
ENST00000644585.1:c.1904G>C	ENSP00000495954.1:p.Trp635Ser
ENST00000645074.1:c.1400G>C	ENSP00000496573.1:p.Trp467Ser
ENST00000645245.1:c.1814G>C	ENSP00000495695.1:p.Trp605Ser
ENST00000645539.1:n.248G>C
ENST00000645791.1:c.1814G>C	ENSP00000494906.1:p.Trp605Ser
ENST00000646690.1:n.59G>C
ENST00000646697.1:c.2067G>C
ENST00000647058.1:n.600G>C
ENST00000647349.1:n.1355G>C
ENST00000647532.1:n.5810G>C
ENST00000279451.8:c.2051G>C	ENSP00000279451.4:p.Trp684Ser
ENST00000379510.3:c.2051G>C	ENSP00000368824.3:p.Trp684Ser
ENST00000425654.6:c.1961G>C	ENSP00000397906.2:p.Trp654Ser
ENST00000543067.5:c.1904G>C	ENSP00000444633.1:p.Trp635Ser
NM_001168647.1:c.1961G>C	NP_001162118.1:p.Trp654Ser
NM_001168648.1:c.2051G>C	NP_001162119.1:p.Trp684Ser
NM_001168649.1:c.1904G>C	NP_001162120.1:p.Trp635Ser
NM_014927.3:c.2051G>C	NP_055742.2:p.Trp684Ser
XM_011545471.1:c.1961G>C	XP_011543773.1:p.Trp654Ser
XM_011545472.1:c.1904G>C	XP_011543774.1:p.Trp635Ser
NM_001168647.2:c.1961G>C	NP_001162118.1:p.Trp654Ser
NM_001168648.2:c.2051G>C	NP_001162119.1:p.Trp684Ser
NM_001168649.2:c.1904G>C	NP_001162120.1:p.Trp635Ser
NM_001330770.1:c.1904G>C	NP_001317699.1:p.Trp635Ser
NM_001330771.1:c.1814G>C	NP_001317700.1:p.Trp605Ser
NM_001330772.1:c.1814G>C	NP_001317701.1:p.Trp605Ser
NM_001330773.1:c.1961G>C	NP_001317702.1:p.Trp654Ser
NM_014927.4:c.2051G>C	NP_055742.2:p.Trp684Ser
XM_011545471.3:c.1961G>C	XP_011543773.1:p.Trp654Ser
XM_011545472.3:c.1904G>C	XP_011543774.1:p.Trp635Ser
XM_017029358.2:c.1814G>C	XP_016884847.1:p.Trp605Ser
NM_014927.5:c.2051G>C MANE Select	NP_055742.2:p.Trp684Ser
NM_001168647.3:c.1961G>C	NP_001162118.1:p.Trp654Ser
NM_001168648.3:c.2051G>C	NP_001162119.1:p.Trp684Ser
NM_001168649.3:c.1904G>C	NP_001162120.1:p.Trp635Ser
NM_001330770.2:c.1904G>C	NP_001317699.1:p.Trp635Ser
NM_001330771.2:c.1814G>C	NP_001317700.1:p.Trp605Ser
NM_001330772.2:c.1814G>C	NP_001317701.1:p.Trp605Ser
NM_001330773.2:c.1961G>C	NP_001317702.1:p.Trp654Ser