Canonical Allele Identifier: CA10366858
Gene: CNKSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.21652342C>T , CM000685.2:g.21652342C>T GRCh38
NC_000023.10:g.21670460C>T , CM000685.1:g.21670460C>T GRCh37
NC_000023.9:g.21580381C>T NCBI36
NG_016266.1:g.282925C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014927.5:c.2926C>T MANE Select NP_055742.2:p.Leu976=
ENST00000379510.5:c.2926C>T MANE Select ENSP00000368824.3:p.Leu976=
NM_001168647.1:c.2836C>T NP_001162118.1:p.Leu946=
NM_001168647.2:c.2836C>T NP_001162118.1:p.Leu946=
NM_001168647.3:c.2836C>T NP_001162118.1:p.Leu946=
NM_001330770.1:c.2779C>T NP_001317699.1:p.Leu927=
NM_001330770.2:c.2779C>T NP_001317699.1:p.Leu927=
NM_001330772.1:c.2689C>T NP_001317701.1:p.Leu897=
NM_001330772.2:c.2689C>T NP_001317701.1:p.Leu897=
NM_014927.3:c.2926C>T NP_055742.2:p.Leu976=
NM_014927.4:c.2926C>T NP_055742.2:p.Leu976=
ENST00000379510.3:c.2926C>T ENSP00000368824.3:p.Leu976=
ENST00000425654.6:c.2836C>T ENSP00000397906.2:p.Leu946=
ENST00000425654.7:c.2836C>T ENSP00000397906.2:p.Leu946=
ENST00000642853.1:n.2704C>T
ENST00000643156.1:c.1758C>T
ENST00000643484.1:n.2634C>T
ENST00000644075.1:n.2292C>T
ENST00000644295.1:c.2851C>T ENSP00000495501.1:p.Leu951=
ENST00000644585.1:c.2779C>T ENSP00000495954.1:p.Leu927=
ENST00000645238.1:n.755C>T
ENST00000645245.1:c.2689C>T ENSP00000495695.1:p.Leu897=
ENST00000645539.1:n.1123C>T
ENST00000646690.1:n.934C>T
ENST00000647532.1:n.6685C>T