Canonical Allele Identifier: CA509340288

Gene: CSNK2A1

Linked Data

• MyVariant Identifiers: chr20:g.476444G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.495800G>T , CM000682.2:g.495800G>T	GRCh38
NC_000020.10:g.476444G>T , CM000682.1:g.476444G>T	GRCh37
NC_000020.9:g.424444G>T	NCBI36
NG_011970.1:g.53039C>A
NG_011970.2:g.53039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217244.9:c.429C>A MANE Select	ENSP00000217244.3:p.Ala143=
ENST00000349736.10:c.21C>A	ENSP00000339247.6:p.Ala7=
ENST00000400217.7:c.429C>A	ENSP00000383076.2:p.Ala143=
ENST00000400227.8:c.429C>A	ENSP00000383086.3:p.Ala143=
ENST00000460062.7:c.21C>A	ENSP00000477147.2:p.Ala7=
ENST00000609525.2:c.429C>A	ENSP00000476547.2:p.Ala143=
ENST00000642689.1:c.378C>A	ENSP00000495414.1:p.Ala126=
ENST00000643600.1:c.429C>A	ENSP00000494038.1:p.Ala143=
ENST00000643602.1:n.448C>A
ENST00000643641.1:n.479C>A
ENST00000643660.1:c.429C>A	ENSP00000495248.1:p.Ala143=
ENST00000643680.1:c.429C>A	ENSP00000493704.1:p.Ala143=
ENST00000643700.1:n.1106C>A
ENST00000643968.1:c.*181C>A	ENSP00000495139.1:n.*181C>A
ENST00000643980.1:n.1322C>A
ENST00000644003.1:c.21C>A	ENSP00000495387.1:p.Ala7=
ENST00000644170.1:n.596C>A
ENST00000644177.1:c.327C>A	ENSP00000495079.1:p.Ala109=
ENST00000644448.1:n.929C>A
ENST00000644710.1:c.378C>A	ENSP00000493791.1:p.Ala126=
ENST00000644885.1:c.426+1921C>A	ENSP00000496146.1:n.426+1921C>A
ENST00000645234.1:c.429C>A	ENSP00000494288.1:p.Ala143=
ENST00000645249.1:c.*502C>A	ENSP00000496152.1:n.*502C>A
ENST00000645260.1:c.318C>A	ENSP00000493931.1:p.Ala106=
ENST00000645623.1:c.429C>A	ENSP00000495998.1:p.Ala143=
ENST00000645768.1:n.1056C>A
ENST00000645840.1:c.*247C>A	ENSP00000494445.1:n.*247C>A
ENST00000645910.1:c.*181C>A	ENSP00000493697.1:n.*181C>A
ENST00000646305.1:c.429C>A	ENSP00000495902.1:p.Ala143=
ENST00000646477.1:c.21C>A	ENSP00000495439.1:p.Ala7=
ENST00000646561.1:c.429C>A	ENSP00000496569.1:p.Ala143=
ENST00000646814.1:c.429C>A	ENSP00000495422.1:p.Ala143=
ENST00000647026.1:c.429C>A	ENSP00000494370.1:p.Ala143=
ENST00000647155.1:n.594C>A
ENST00000647348.1:c.429C>A	ENSP00000495912.1:p.Ala143=
ENST00000217244.7:c.429C>A	ENSP00000217244.3:p.Ala143=
ENST00000349736.9:c.429C>A	ENSP00000339247.5:p.Ala143=
ENST00000400217.6:c.21C>A	ENSP00000383076.1:p.Ala7=
ENST00000400227.7:c.429C>A	ENSP00000383086.3:p.Ala143=
ENST00000460062.6:c.21C>A	ENSP00000477147.1:p.Ala7=
ENST00000619188.4:c.429C>A	ENSP00000479630.1:p.Ala143=
NM_001895.3:c.429C>A	NP_001886.1:p.Ala143=
NM_177559.2:c.429C>A	NP_808227.1:p.Ala143=
NM_177560.2:c.21C>A	NP_808228.1:p.Ala7=
XM_011529175.1:c.429C>A	XP_011527477.1:p.Ala143=
XM_011529176.1:c.21C>A	XP_011527478.1:p.Ala7=
NM_001362770.1:c.429C>A	NP_001349699.1:p.Ala143=
NM_001362771.1:c.429C>A	NP_001349700.1:p.Ala143=
NM_177559.3:c.429C>A MANE Select	NP_808227.1:p.Ala143=
NM_001362770.2:c.429C>A	NP_001349699.1:p.Ala143=
NM_001362771.2:c.429C>A	NP_001349700.1:p.Ala143=
NM_001895.4:c.429C>A	NP_001886.1:p.Ala143=
NM_177560.3:c.21C>A	NP_808228.1:p.Ala7=