Canonical Allele Identifier: CA16608001
Gene: CSNK2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 392940
ClinVar RCV Id: RCV000431425
dbSNP Id: rs1057524708
MyVariant Identifiers: chr20:g.478364C>A (hg19) chr20:g.497720C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.497720C>A , CM000682.2:g.497720C>A GRCh38
NC_000020.10:g.478364C>A , CM000682.1:g.478364C>A GRCh37
NC_000020.9:g.426364C>A NCBI36
NG_011970.1:g.51119G>T
NG_011970.2:g.51119G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217244.9:c.426+1G>T MANE Select ENSP00000217244.3:n.426+1G>T
ENST00000349736.10:c.18+1G>T ENSP00000339247.6:n.18+1G>T
ENST00000400217.7:c.426+1G>T ENSP00000383076.2:n.426+1G>T
ENST00000400227.8:c.426+1G>T ENSP00000383086.3:n.426+1G>T
ENST00000460062.7:c.18+1G>T ENSP00000477147.2:n.18+1G>T
ENST00000609525.2:c.426+1G>T ENSP00000476547.2:n.426+1G>T
ENST00000642689.1:c.375+1G>T ENSP00000495414.1:n.375+1G>T
ENST00000643600.1:c.426+1G>T ENSP00000494038.1:n.426+1G>T
ENST00000643602.1:n.445+1G>T
ENST00000643641.1:n.476+1G>T
ENST00000643660.1:c.426+1G>T ENSP00000495248.1:n.426+1G>T
ENST00000643680.1:c.426+1G>T ENSP00000493704.1:n.426+1G>T
ENST00000643700.1:n.1103+1G>T
ENST00000643968.1:c.*178+1G>T ENSP00000495139.1:n.*178+1G>T
ENST00000643980.1:n.1319+1G>T
ENST00000644003.1:c.18+1G>T ENSP00000495387.1:n.18+1G>T
ENST00000644170.1:n.593+1G>T
ENST00000644177.1:c.324+1G>T ENSP00000495079.1:n.324+1G>T
ENST00000644710.1:c.375+1G>T ENSP00000493791.1:n.375+1G>T
ENST00000644885.1:c.426+1G>T ENSP00000496146.1:n.426+1G>T
ENST00000645234.1:c.426+1G>T ENSP00000494288.1:n.426+1G>T
ENST00000645249.1:c.*499+1G>T ENSP00000496152.1:n.*499+1G>T
ENST00000645260.1:c.316-1918G>T ENSP00000493931.1:n.316-1918G>T
ENST00000645623.1:c.426+1G>T ENSP00000495998.1:n.426+1G>T
ENST00000645768.1:n.1053+1G>T
ENST00000645840.1:c.*244+1G>T ENSP00000494445.1:n.*244+1G>T
ENST00000645910.1:c.*178+1G>T ENSP00000493697.1:n.*178+1G>T
ENST00000646305.1:c.426+1G>T ENSP00000495902.1:n.426+1G>T
ENST00000646477.1:c.18+1G>T ENSP00000495439.1:n.18+1G>T
ENST00000646561.1:c.426+1G>T ENSP00000496569.1:n.426+1G>T
ENST00000646814.1:c.426+1G>T ENSP00000495422.1:n.426+1G>T
ENST00000647026.1:c.426+1G>T ENSP00000494370.1:n.426+1G>T
ENST00000647155.1:n.591+1G>T
ENST00000647348.1:c.426+1G>T ENSP00000495912.1:n.426+1G>T
ENST00000217244.7:c.426+1G>T ENSP00000217244.3:n.426+1G>T
ENST00000349736.9:c.426+1G>T ENSP00000339247.5:n.426+1G>T
ENST00000400217.6:c.18+1G>T ENSP00000383076.1:n.18+1G>T
ENST00000400227.7:c.426+1G>T ENSP00000383086.3:n.426+1G>T
ENST00000460062.6:c.18+1G>T ENSP00000477147.1:n.18+1G>T
ENST00000619188.4:c.426+1G>T ENSP00000479630.1:n.426+1G>T
NM_001895.3:c.426+1G>T NP_001886.1:n.426+1G>T
NM_177559.2:c.426+1G>T NP_808227.1:n.426+1G>T
NM_177560.2:c.18+1G>T NP_808228.1:n.18+1G>T
XM_011529175.1:c.426+1G>T XP_011527477.1:n.426+1G>T
XM_011529176.1:c.18+1G>T XP_011527478.1:n.18+1G>T
NM_001362770.1:c.426+1G>T NP_001349699.1:n.426+1G>T
NM_001362771.1:c.426+1G>T NP_001349700.1:n.426+1G>T
NM_177559.3:c.426+1G>T MANE Select NP_808227.1:n.426+1G>T
NM_001362770.2:c.426+1G>T NP_001349699.1:n.426+1G>T
NM_001362771.2:c.426+1G>T NP_001349700.1:n.426+1G>T
NM_001895.4:c.426+1G>T NP_001886.1:n.426+1G>T
NM_177560.3:c.18+1G>T NP_808228.1:n.18+1G>T
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