Canonical Allele Identifier: CA2345222521
Gene: CSNK2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.496068_496071delinsGCAC , CM000682.2:g.496068_496071delinsGCAC GRCh38
NC_000020.10:g.476712_476715delinsGCAC , CM000682.1:g.476712_476715delinsGCAC GRCh37
NC_000020.9:g.424712_424715delinsGCAC NCBI36
NG_011970.1:g.52768_52771delinsGTGC
NG_011970.2:g.52768_52771delinsGTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000217244.9:c.427-269_427-266delinsGTGC MANE Select ENSP00000217244.3:n.427-269_427-266delinsGTGC
ENST00000349736.10:c.19-269_19-266delinsGTGC ENSP00000339247.6:n.19-269_19-266delinsGTGC
ENST00000400217.7:c.427-269_427-266delinsGTGC ENSP00000383076.2:n.427-269_427-266delinsGTGC
ENST00000400227.8:c.427-269_427-266delinsGTGC ENSP00000383086.3:n.427-269_427-266delinsGTGC
ENST00000460062.7:c.19-269_19-266delinsGTGC ENSP00000477147.2:n.19-269_19-266delinsGTGC
ENST00000609525.2:c.427-269_427-266delinsGTGC ENSP00000476547.2:n.427-269_427-266delinsGTGC
ENST00000642689.1:c.376-269_376-266delinsGTGC ENSP00000495414.1:n.376-269_376-266delinsGTGC
ENST00000643600.1:c.427-269_427-266delinsGTGC ENSP00000494038.1:n.427-269_427-266delinsGTGC
ENST00000643602.1:n.446-269_446-266delinsGTGC
ENST00000643641.1:n.477-269_477-266delinsGTGC
ENST00000643660.1:c.427-269_427-266delinsGTGC ENSP00000495248.1:n.427-269_427-266delinsGTGC
ENST00000643680.1:c.427-269_427-266delinsGTGC ENSP00000493704.1:n.427-269_427-266delinsGTGC
ENST00000643700.1:n.1104-269_1104-266delinsGTGC
ENST00000643968.1:c.*179-269_*179-266delinsGTGC ENSP00000495139.1:n.*179-269_*179-266delinsGTGC
ENST00000643980.1:n.1320-269_1320-266delinsGTGC
ENST00000644003.1:c.19-269_19-266delinsGTGC ENSP00000495387.1:n.19-269_19-266delinsGTGC
ENST00000644170.1:n.594-269_594-266delinsGTGC
ENST00000644177.1:c.325-269_325-266delinsGTGC ENSP00000495079.1:n.325-269_325-266delinsGTGC
ENST00000644448.1:n.658_661delinsGTGC
ENST00000644710.1:c.376-269_376-266delinsGTGC ENSP00000493791.1:n.376-269_376-266delinsGTGC
ENST00000644885.1:c.426+1650_426+1653delinsGTGC ENSP00000496146.1:n.426+1650_426+1653delinsGTGC
ENST00000645234.1:c.427-269_427-266delinsGTGC ENSP00000494288.1:n.427-269_427-266delinsGTGC
ENST00000645249.1:c.*500-269_*500-266delinsGTGC ENSP00000496152.1:n.*500-269_*500-266delinsGTGC
ENST00000645260.1:c.316-269_316-266delinsGTGC ENSP00000493931.1:n.316-269_316-266delinsGTGC
ENST00000645623.1:c.427-269_427-266delinsGTGC ENSP00000495998.1:n.427-269_427-266delinsGTGC
ENST00000645768.1:n.1054-269_1054-266delinsGTGC
ENST00000645840.1:c.*245-269_*245-266delinsGTGC ENSP00000494445.1:n.*245-269_*245-266delinsGTGC
ENST00000645910.1:c.*179-269_*179-266delinsGTGC ENSP00000493697.1:n.*179-269_*179-266delinsGTGC
ENST00000646305.1:c.427-269_427-266delinsGTGC ENSP00000495902.1:n.427-269_427-266delinsGTGC
ENST00000646477.1:c.19-269_19-266delinsGTGC ENSP00000495439.1:n.19-269_19-266delinsGTGC
ENST00000646561.1:c.427-269_427-266delinsGTGC ENSP00000496569.1:n.427-269_427-266delinsGTGC
ENST00000646814.1:c.427-269_427-266delinsGTGC ENSP00000495422.1:n.427-269_427-266delinsGTGC
ENST00000647026.1:c.427-269_427-266delinsGTGC ENSP00000494370.1:n.427-269_427-266delinsGTGC
ENST00000647155.1:n.592-269_592-266delinsGTGC
ENST00000647348.1:c.427-269_427-266delinsGTGC ENSP00000495912.1:n.427-269_427-266delinsGTGC
ENST00000217244.7:c.427-269_427-266delinsGTGC ENSP00000217244.3:n.427-269_427-266delinsGTGC
ENST00000349736.9:c.427-269_427-266delinsGTGC ENSP00000339247.5:n.427-269_427-266delinsGTGC
ENST00000400217.6:c.19-269_19-266delinsGTGC ENSP00000383076.1:n.19-269_19-266delinsGTGC
ENST00000400227.7:c.427-269_427-266delinsGTGC ENSP00000383086.3:n.427-269_427-266delinsGTGC
ENST00000460062.6:c.19-269_19-266delinsGTGC ENSP00000477147.1:n.19-269_19-266delinsGTGC
ENST00000619188.4:c.427-269_427-266delinsGTGC ENSP00000479630.1:n.427-269_427-266delinsGTGC
NM_001895.3:c.427-269_427-266delinsGTGC NP_001886.1:n.427-269_427-266delinsGTGC
NM_177559.2:c.427-269_427-266delinsGTGC NP_808227.1:n.427-269_427-266delinsGTGC
NM_177560.2:c.19-269_19-266delinsGTGC NP_808228.1:n.19-269_19-266delinsGTGC
XM_011529175.1:c.427-269_427-266delinsGTGC XP_011527477.1:n.427-269_427-266delinsGTGC
XM_011529176.1:c.19-269_19-266delinsGTGC XP_011527478.1:n.19-269_19-266delinsGTGC
NM_001362770.1:c.427-269_427-266delinsGTGC NP_001349699.1:n.427-269_427-266delinsGTGC
NM_001362771.1:c.427-269_427-266delinsGTGC NP_001349700.1:n.427-269_427-266delinsGTGC
NM_177559.3:c.427-269_427-266delinsGTGC MANE Select NP_808227.1:n.427-269_427-266delinsGTGC
NM_001362770.2:c.427-269_427-266delinsGTGC NP_001349699.1:n.427-269_427-266delinsGTGC
NM_001362771.2:c.427-269_427-266delinsGTGC NP_001349700.1:n.427-269_427-266delinsGTGC
NM_001895.4:c.427-269_427-266delinsGTGC NP_001886.1:n.427-269_427-266delinsGTGC
NM_177560.3:c.19-269_19-266delinsGTGC NP_808228.1:n.19-269_19-266delinsGTGC