Canonical Allele Identifier: CA2345222393
Gene: CSNK2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.495734A= , CM000682.2:g.495734A= GRCh38
NC_000020.10:g.476378A= , CM000682.1:g.476378A= GRCh37
NC_000020.9:g.424378A= NCBI36
NG_011970.1:g.53105T=
NG_011970.2:g.53105T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217244.9:c.495T= MANE Select ENSP00000217244.3:p.Asp165=
ENST00000349736.10:c.87T= ENSP00000339247.6:p.Asp29=
ENST00000400217.7:c.495T= ENSP00000383076.2:p.Asp165=
ENST00000400227.8:c.495T= ENSP00000383086.3:p.Asp165=
ENST00000460062.7:c.87T= ENSP00000477147.2:p.Asp29=
ENST00000642689.1:c.444T= ENSP00000495414.1:p.Asp148=
ENST00000643600.1:c.495T= ENSP00000494038.1:p.Asp165=
ENST00000643602.1:n.514T=
ENST00000643641.1:n.545T=
ENST00000643660.1:c.495T= ENSP00000495248.1:p.Asp165=
ENST00000643680.1:c.495T= ENSP00000493704.1:p.Asp165=
ENST00000643700.1:n.1172T=
ENST00000643968.1:c.*247T= ENSP00000495139.1:n.*247T=
ENST00000643980.1:n.1388T=
ENST00000644003.1:c.87T= ENSP00000495387.1:p.Asp29=
ENST00000644170.1:n.662T=
ENST00000644177.1:c.393T= ENSP00000495079.1:p.Asp131=
ENST00000644448.1:n.995T=
ENST00000644710.1:c.444T= ENSP00000493791.1:p.Asp148=
ENST00000644885.1:c.426+1987T= ENSP00000496146.1:n.426+1987T=
ENST00000645234.1:c.495T= ENSP00000494288.1:p.Asp165=
ENST00000645249.1:c.*568T= ENSP00000496152.1:n.*568T=
ENST00000645260.1:c.384T= ENSP00000493931.1:p.Asp128=
ENST00000645623.1:c.495T= ENSP00000495998.1:p.Asp165=
ENST00000645768.1:n.1122T=
ENST00000645840.1:c.*313T= ENSP00000494445.1:n.*313T=
ENST00000645910.1:c.*247T= ENSP00000493697.1:n.*247T=
ENST00000646305.1:c.495T= ENSP00000495902.1:p.Asp165=
ENST00000646477.1:c.87T= ENSP00000495439.1:p.Asp29=
ENST00000646561.1:c.495T= ENSP00000496569.1:p.Asp165=
ENST00000646814.1:c.495T= ENSP00000495422.1:p.Asp165=
ENST00000647026.1:c.495T= ENSP00000494370.1:p.Asp165=
ENST00000647155.1:n.660T=
ENST00000647348.1:c.495T= ENSP00000495912.1:p.Asp165=
ENST00000217244.7:c.495T= ENSP00000217244.3:p.Asp165=
ENST00000349736.9:c.495T= ENSP00000339247.5:p.Asp165=
ENST00000400217.6:c.87T= ENSP00000383076.1:p.Asp29=
ENST00000400227.7:c.495T= ENSP00000383086.3:p.Asp165=
ENST00000619188.4:c.495T= ENSP00000479630.1:p.Asp165=
NM_001895.3:c.495T= NP_001886.1:p.Asp165=
NM_177559.2:c.495T= NP_808227.1:p.Asp165=
NM_177560.2:c.87T= NP_808228.1:p.Asp29=
XM_011529175.1:c.495T= XP_011527477.1:p.Asp165=
XM_011529176.1:c.87T= XP_011527478.1:p.Asp29=
NM_001362770.1:c.495T= NP_001349699.1:p.Asp165=
NM_001362771.1:c.495T= NP_001349700.1:p.Asp165=
NM_177559.3:c.495T= MANE Select NP_808227.1:p.Asp165=
NM_001362770.2:c.495T= NP_001349699.1:p.Asp165=
NM_001362771.2:c.495T= NP_001349700.1:p.Asp165=
NM_001895.4:c.495T= NP_001886.1:p.Asp165=
NM_177560.3:c.87T= NP_808228.1:p.Asp29=