Canonical Allele Identifier: CA2345222467
Gene: CSNK2A1 HGNC NCBI

Linked Data

dbSNP Id: rs2018338828

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.495930C>T , CM000682.2:g.495930C>T GRCh38
NC_000020.10:g.476574C>T , CM000682.1:g.476574C>T GRCh37
NC_000020.9:g.424574C>T NCBI36
NG_011970.1:g.52909G>A
NG_011970.2:g.52909G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217244.9:c.427-128G>A MANE Select ENSP00000217244.3:n.427-128G>A
ENST00000349736.10:c.19-128G>A ENSP00000339247.6:n.19-128G>A
ENST00000400217.7:c.427-128G>A ENSP00000383076.2:n.427-128G>A
ENST00000400227.8:c.427-128G>A ENSP00000383086.3:n.427-128G>A
ENST00000460062.7:c.19-128G>A ENSP00000477147.2:n.19-128G>A
ENST00000609525.2:c.427-128G>A ENSP00000476547.2:n.427-128G>A
ENST00000642689.1:c.376-128G>A ENSP00000495414.1:n.376-128G>A
ENST00000643600.1:c.427-128G>A ENSP00000494038.1:n.427-128G>A
ENST00000643602.1:n.446-128G>A
ENST00000643641.1:n.477-128G>A
ENST00000643660.1:c.427-128G>A ENSP00000495248.1:n.427-128G>A
ENST00000643680.1:c.427-128G>A ENSP00000493704.1:n.427-128G>A
ENST00000643700.1:n.1104-128G>A
ENST00000643968.1:c.*179-128G>A ENSP00000495139.1:n.*179-128G>A
ENST00000643980.1:n.1320-128G>A
ENST00000644003.1:c.19-128G>A ENSP00000495387.1:n.19-128G>A
ENST00000644170.1:n.594-128G>A
ENST00000644177.1:c.325-128G>A ENSP00000495079.1:n.325-128G>A
ENST00000644448.1:n.799G>A
ENST00000644710.1:c.376-128G>A ENSP00000493791.1:n.376-128G>A
ENST00000644885.1:c.426+1791G>A ENSP00000496146.1:n.426+1791G>A
ENST00000645234.1:c.427-128G>A ENSP00000494288.1:n.427-128G>A
ENST00000645249.1:c.*500-128G>A ENSP00000496152.1:n.*500-128G>A
ENST00000645260.1:c.316-128G>A ENSP00000493931.1:n.316-128G>A
ENST00000645623.1:c.427-128G>A ENSP00000495998.1:n.427-128G>A
ENST00000645768.1:n.1054-128G>A
ENST00000645840.1:c.*245-128G>A ENSP00000494445.1:n.*245-128G>A
ENST00000645910.1:c.*179-128G>A ENSP00000493697.1:n.*179-128G>A
ENST00000646305.1:c.427-128G>A ENSP00000495902.1:n.427-128G>A
ENST00000646477.1:c.19-128G>A ENSP00000495439.1:n.19-128G>A
ENST00000646561.1:c.427-128G>A ENSP00000496569.1:n.427-128G>A
ENST00000646814.1:c.427-128G>A ENSP00000495422.1:n.427-128G>A
ENST00000647026.1:c.427-128G>A ENSP00000494370.1:n.427-128G>A
ENST00000647155.1:n.592-128G>A
ENST00000647348.1:c.427-128G>A ENSP00000495912.1:n.427-128G>A
ENST00000217244.7:c.427-128G>A ENSP00000217244.3:n.427-128G>A
ENST00000349736.9:c.427-128G>A ENSP00000339247.5:n.427-128G>A
ENST00000400217.6:c.19-128G>A ENSP00000383076.1:n.19-128G>A
ENST00000400227.7:c.427-128G>A ENSP00000383086.3:n.427-128G>A
ENST00000460062.6:c.19-128G>A ENSP00000477147.1:n.19-128G>A
ENST00000619188.4:c.427-128G>A ENSP00000479630.1:n.427-128G>A
NM_001895.3:c.427-128G>A NP_001886.1:n.427-128G>A
NM_177559.2:c.427-128G>A NP_808227.1:n.427-128G>A
NM_177560.2:c.19-128G>A NP_808228.1:n.19-128G>A
XM_011529175.1:c.427-128G>A XP_011527477.1:n.427-128G>A
XM_011529176.1:c.19-128G>A XP_011527478.1:n.19-128G>A
NM_001362770.1:c.427-128G>A NP_001349699.1:n.427-128G>A
NM_001362771.1:c.427-128G>A NP_001349700.1:n.427-128G>A
NM_177559.3:c.427-128G>A MANE Select NP_808227.1:n.427-128G>A
NM_001362770.2:c.427-128G>A NP_001349699.1:n.427-128G>A
NM_001362771.2:c.427-128G>A NP_001349700.1:n.427-128G>A
NM_001895.4:c.427-128G>A NP_001886.1:n.427-128G>A
NM_177560.3:c.19-128G>A NP_808228.1:n.19-128G>A