Canonical Allele Identifier: CA407932868

Gene: CSNK2A1

Linked Data

• MyVariant Identifiers: chr20:g.476377G>A (hg19) ; chr20:g.495733G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.495733G>A , CM000682.2:g.495733G>A	GRCh38
NC_000020.10:g.476377G>A , CM000682.1:g.476377G>A	GRCh37
NC_000020.9:g.424377G>A	NCBI36
NG_011970.1:g.53106C>T
NG_011970.2:g.53106C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217244.9:c.496C>T MANE Select	ENSP00000217244.3:p.His166Tyr
ENST00000349736.10:c.88C>T	ENSP00000339247.6:p.His30Tyr
ENST00000400217.7:c.496C>T	ENSP00000383076.2:p.His166Tyr
ENST00000400227.8:c.496C>T	ENSP00000383086.3:p.His166Tyr
ENST00000460062.7:c.88C>T	ENSP00000477147.2:p.His30Tyr
ENST00000642689.1:c.445C>T	ENSP00000495414.1:p.His149Tyr
ENST00000643600.1:c.496C>T	ENSP00000494038.1:p.His166Tyr
ENST00000643602.1:n.515C>T
ENST00000643641.1:n.546C>T
ENST00000643660.1:c.496C>T	ENSP00000495248.1:p.His166Tyr
ENST00000643680.1:c.496C>T	ENSP00000493704.1:p.His166Tyr
ENST00000643700.1:n.1173C>T
ENST00000643968.1:c.*248C>T	ENSP00000495139.1:n.*248C>T
ENST00000643980.1:n.1389C>T
ENST00000644003.1:c.88C>T	ENSP00000495387.1:p.His30Tyr
ENST00000644170.1:n.663C>T
ENST00000644177.1:c.394C>T
ENST00000644448.1:n.996C>T
ENST00000644710.1:c.445C>T	ENSP00000493791.1:p.His149Tyr
ENST00000644885.1:c.426+1988C>T	ENSP00000496146.1:n.426+1988C>T
ENST00000645234.1:c.496C>T	ENSP00000494288.1:p.His166Tyr
ENST00000645249.1:c.*569C>T	ENSP00000496152.1:n.*569C>T
ENST00000645260.1:c.385C>T	ENSP00000493931.1:p.His129Tyr
ENST00000645623.1:c.496C>T	ENSP00000495998.1:p.His166Tyr
ENST00000645768.1:n.1123C>T
ENST00000645840.1:c.*314C>T	ENSP00000494445.1:n.*314C>T
ENST00000645910.1:c.*248C>T	ENSP00000493697.1:n.*248C>T
ENST00000646305.1:c.496C>T	ENSP00000495902.1:p.His166Tyr
ENST00000646477.1:c.88C>T	ENSP00000495439.1:p.His30Tyr
ENST00000646561.1:c.496C>T	ENSP00000496569.1:p.His166Tyr
ENST00000646814.1:c.496C>T	ENSP00000495422.1:p.His166Tyr
ENST00000647026.1:c.496C>T	ENSP00000494370.1:p.His166Tyr
ENST00000647155.1:n.661C>T
ENST00000647348.1:c.496C>T	ENSP00000495912.1:p.His166Tyr
ENST00000217244.7:c.496C>T	ENSP00000217244.3:p.His166Tyr
ENST00000349736.9:c.496C>T	ENSP00000339247.5:p.His166Tyr
ENST00000400217.6:c.88C>T	ENSP00000383076.1:p.His30Tyr
ENST00000400227.7:c.496C>T	ENSP00000383086.3:p.His166Tyr
ENST00000619188.4:c.496C>T	ENSP00000479630.1:p.His166Tyr
NM_001895.3:c.496C>T	NP_001886.1:p.His166Tyr
NM_177559.2:c.496C>T	NP_808227.1:p.His166Tyr
NM_177560.2:c.88C>T	NP_808228.1:p.His30Tyr
XM_011529175.1:c.496C>T	XP_011527477.1:p.His166Tyr
XM_011529176.1:c.88C>T	XP_011527478.1:p.His30Tyr
NM_001362770.1:c.496C>T	NP_001349699.1:p.His166Tyr
NM_001362771.1:c.496C>T	NP_001349700.1:p.His166Tyr
NM_177559.3:c.496C>T MANE Select	NP_808227.1:p.His166Tyr
NM_001362770.2:c.496C>T	NP_001349699.1:p.His166Tyr
NM_001362771.2:c.496C>T	NP_001349700.1:p.His166Tyr
NM_001895.4:c.496C>T	NP_001886.1:p.His166Tyr
NM_177560.3:c.88C>T	NP_808228.1:p.His30Tyr