Canonical Allele Identifier: CA509340711

Gene: CSNK2A1

Linked Data

• MyVariant Identifiers: chr20:g.485836G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.505192G>T , CM000682.2:g.505192G>T	GRCh38
NC_000020.10:g.485836G>T , CM000682.1:g.485836G>T	GRCh37
NC_000020.9:g.433836G>T	NCBI36
NG_011970.1:g.43647C>A
NG_011970.2:g.43647C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217244.9:c.139C>A MANE Select	ENSP00000217244.3:p.Arg47=
ENST00000349736.10:c.-270C>A	ENSP00000339247.6:n.-270C>A
ENST00000400217.7:c.139C>A	ENSP00000383076.2:p.Arg47=
ENST00000400227.8:c.139C>A	ENSP00000383086.3:p.Arg47=
ENST00000460062.7:c.-270C>A	ENSP00000477147.2:n.-270C>A
ENST00000608066.6:c.139C>A	ENSP00000476486.2:p.Arg47=
ENST00000609525.2:c.139C>A	ENSP00000476547.2:p.Arg47=
ENST00000609606.6:n.367C>A
ENST00000642160.1:c.139C>A	ENSP00000496115.1:p.Arg47=
ENST00000642689.1:c.139C>A	ENSP00000495414.1:p.Arg47=
ENST00000643600.1:c.139C>A	ENSP00000494038.1:p.Arg47=
ENST00000643660.1:c.139C>A	ENSP00000495248.1:p.Arg47=
ENST00000643680.1:c.139C>A	ENSP00000493704.1:p.Arg47=
ENST00000643700.1:n.289C>A
ENST00000643968.1:c.139C>A	ENSP00000495139.1:p.Arg47=
ENST00000644003.1:c.-376C>A	ENSP00000495387.1:n.-376C>A
ENST00000644170.1:n.306C>A
ENST00000644177.1:c.139C>A	ENSP00000495079.1:p.Arg47=
ENST00000644710.1:c.139C>A	ENSP00000493791.1:p.Arg47=
ENST00000644885.1:c.139C>A	ENSP00000496146.1:p.Arg47=
ENST00000645091.1:c.139C>A	ENSP00000495942.1:p.Arg47=
ENST00000645187.1:c.139C>A	ENSP00000496232.1:p.Arg47=
ENST00000645234.1:c.139C>A	ENSP00000494288.1:p.Arg47=
ENST00000645249.1:c.139C>A	ENSP00000496152.1:p.Arg47=
ENST00000645260.1:c.139C>A	ENSP00000493931.1:p.Arg47=
ENST00000645623.1:c.139C>A	ENSP00000495998.1:p.Arg47=
ENST00000645641.1:n.86C>A
ENST00000645840.1:c.139C>A	ENSP00000494445.1:p.Arg47=
ENST00000645910.1:c.139C>A	ENSP00000493697.1:p.Arg47=
ENST00000646305.1:c.139C>A	ENSP00000495902.1:p.Arg47=
ENST00000646443.1:n.44C>A
ENST00000646477.1:c.-404C>A	ENSP00000495439.1:n.-404C>A
ENST00000646561.1:c.139C>A	ENSP00000496569.1:p.Arg47=
ENST00000646814.1:c.139C>A	ENSP00000495422.1:p.Arg47=
ENST00000646908.1:c.139C>A	ENSP00000493643.1:p.Arg47=
ENST00000647026.1:c.139C>A	ENSP00000494370.1:p.Arg47=
ENST00000647155.1:n.304C>A
ENST00000647348.1:c.139C>A	ENSP00000495912.1:p.Arg47=
ENST00000217244.7:c.139C>A	ENSP00000217244.3:p.Arg47=
ENST00000349736.9:c.139C>A	ENSP00000339247.5:p.Arg47=
ENST00000400217.6:c.-270C>A	ENSP00000383076.1:n.-270C>A
ENST00000400227.7:c.139C>A	ENSP00000383086.3:p.Arg47=
ENST00000460062.6:c.-376C>A	ENSP00000477147.1:n.-376C>A
ENST00000608066.5:c.139C>A	ENSP00000476486.1:p.Arg47=
ENST00000608490.1:n.150C>A
ENST00000609525.1:c.139C>A	ENSP00000476547.1:p.Arg47=
ENST00000609606.5:n.306C>A
ENST00000619188.4:c.139C>A	ENSP00000479630.1:p.Arg47=
NM_001895.3:c.139C>A	NP_001886.1:p.Arg47=
NM_177559.2:c.139C>A	NP_808227.1:p.Arg47=
NM_177560.2:c.-270C>A	NP_808228.1:n.-270C>A
XM_011529175.1:c.139C>A	XP_011527477.1:p.Arg47=
XM_011529176.1:c.-355C>A	XP_011527478.1:n.-355C>A
NM_001362770.1:c.139C>A	NP_001349699.1:p.Arg47=
NM_001362771.1:c.139C>A	NP_001349700.1:p.Arg47=
NM_177559.3:c.139C>A MANE Select	NP_808227.1:p.Arg47=
NM_001362770.2:c.139C>A	NP_001349699.1:p.Arg47=
NM_001362771.2:c.139C>A	NP_001349700.1:p.Arg47=
NM_001895.4:c.139C>A	NP_001886.1:p.Arg47=
NM_177560.3:c.-270C>A	NP_808228.1:n.-270C>A