Canonical Allele Identifier: CA407933107

Gene: CSNK2A1

Linked Data

• ClinVar Variation Id: 984880
• ClinVar RCV Id: RCV001265461
• dbSNP Id: rs1568512728
• MyVariant Identifiers: chr20:g.476407C>A (hg19) ; chr20:g.495763C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.495763C>A , CM000682.2:g.495763C>A	GRCh38
NC_000020.10:g.476407C>A , CM000682.1:g.476407C>A	GRCh37
NC_000020.9:g.424407C>A	NCBI36
NG_011970.1:g.53076G>T
NG_011970.2:g.53076G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217244.9:c.466G>T MANE Select	ENSP00000217244.3:p.Asp156Tyr
ENST00000349736.10:c.58G>T	ENSP00000339247.6:p.Asp20Tyr
ENST00000400217.7:c.466G>T	ENSP00000383076.2:p.Asp156Tyr
ENST00000400227.8:c.466G>T	ENSP00000383086.3:p.Asp156Tyr
ENST00000460062.7:c.58G>T	ENSP00000477147.2:p.Asp20Tyr
ENST00000642689.1:c.415G>T	ENSP00000495414.1:p.Asp139Tyr
ENST00000643600.1:c.466G>T	ENSP00000494038.1:p.Asp156Tyr
ENST00000643602.1:n.485G>T
ENST00000643641.1:n.516G>T
ENST00000643660.1:c.466G>T	ENSP00000495248.1:p.Asp156Tyr
ENST00000643680.1:c.466G>T	ENSP00000493704.1:p.Asp156Tyr
ENST00000643700.1:n.1143G>T
ENST00000643968.1:c.*218G>T	ENSP00000495139.1:n.*218G>T
ENST00000643980.1:n.1359G>T
ENST00000644003.1:c.58G>T	ENSP00000495387.1:p.Asp20Tyr
ENST00000644170.1:n.633G>T
ENST00000644177.1:c.364G>T	ENSP00000495079.1:p.Asp122Tyr
ENST00000644448.1:n.966G>T
ENST00000644710.1:c.415G>T	ENSP00000493791.1:p.Asp139Tyr
ENST00000644885.1:c.426+1958G>T	ENSP00000496146.1:n.426+1958G>T
ENST00000645234.1:c.466G>T	ENSP00000494288.1:p.Asp156Tyr
ENST00000645249.1:c.*539G>T	ENSP00000496152.1:n.*539G>T
ENST00000645260.1:c.355G>T	ENSP00000493931.1:p.Asp119Tyr
ENST00000645623.1:c.466G>T	ENSP00000495998.1:p.Asp156Tyr
ENST00000645768.1:n.1093G>T
ENST00000645840.1:c.*284G>T	ENSP00000494445.1:n.*284G>T
ENST00000645910.1:c.*218G>T	ENSP00000493697.1:n.*218G>T
ENST00000646305.1:c.466G>T	ENSP00000495902.1:p.Asp156Tyr
ENST00000646477.1:c.58G>T	ENSP00000495439.1:p.Asp20Tyr
ENST00000646561.1:c.466G>T	ENSP00000496569.1:p.Asp156Tyr
ENST00000646814.1:c.466G>T	ENSP00000495422.1:p.Asp156Tyr
ENST00000647026.1:c.466G>T	ENSP00000494370.1:p.Asp156Tyr
ENST00000647155.1:n.631G>T
ENST00000647348.1:c.466G>T	ENSP00000495912.1:p.Asp156Tyr
ENST00000217244.7:c.466G>T	ENSP00000217244.3:p.Asp156Tyr
ENST00000349736.9:c.466G>T	ENSP00000339247.5:p.Asp156Tyr
ENST00000400217.6:c.58G>T	ENSP00000383076.1:p.Asp20Tyr
ENST00000400227.7:c.466G>T	ENSP00000383086.3:p.Asp156Tyr
ENST00000460062.6:c.58G>T	ENSP00000477147.1:p.Asp20Tyr
ENST00000619188.4:c.466G>T	ENSP00000479630.1:p.Asp156Tyr
NM_001895.3:c.466G>T	NP_001886.1:p.Asp156Tyr
NM_177559.2:c.466G>T	NP_808227.1:p.Asp156Tyr
NM_177560.2:c.58G>T	NP_808228.1:p.Asp20Tyr
XM_011529175.1:c.466G>T	XP_011527477.1:p.Asp156Tyr
XM_011529176.1:c.58G>T	XP_011527478.1:p.Asp20Tyr
NM_001362770.1:c.466G>T	NP_001349699.1:p.Asp156Tyr
NM_001362771.1:c.466G>T	NP_001349700.1:p.Asp156Tyr
NM_177559.3:c.466G>T MANE Select	NP_808227.1:p.Asp156Tyr
NM_001362770.2:c.466G>T	NP_001349699.1:p.Asp156Tyr
NM_001362771.2:c.466G>T	NP_001349700.1:p.Asp156Tyr
NM_001895.4:c.466G>T	NP_001886.1:p.Asp156Tyr
NM_177560.3:c.58G>T	NP_808228.1:p.Asp20Tyr