Canonical Allele Identifier: CA407933119

Gene: CSNK2A1

Linked Data

• MyVariant Identifiers: chr20:g.476409C>G (hg19) ; chr20:g.495765C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.495765C>G , CM000682.2:g.495765C>G	GRCh38
NC_000020.10:g.476409C>G , CM000682.1:g.476409C>G	GRCh37
NC_000020.9:g.424409C>G	NCBI36
NG_011970.1:g.53074G>C
NG_011970.2:g.53074G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217244.9:c.464G>C MANE Select	ENSP00000217244.3:p.Arg155Thr
ENST00000349736.10:c.56G>C	ENSP00000339247.6:p.Arg19Thr
ENST00000400217.7:c.464G>C	ENSP00000383076.2:p.Arg155Thr
ENST00000400227.8:c.464G>C	ENSP00000383086.3:p.Arg155Thr
ENST00000460062.7:c.56G>C	ENSP00000477147.2:p.Arg19Thr
ENST00000642689.1:c.413G>C	ENSP00000495414.1:p.Arg138Thr
ENST00000643600.1:c.464G>C	ENSP00000494038.1:p.Arg155Thr
ENST00000643602.1:n.483G>C
ENST00000643641.1:n.514G>C
ENST00000643660.1:c.464G>C	ENSP00000495248.1:p.Arg155Thr
ENST00000643680.1:c.464G>C	ENSP00000493704.1:p.Arg155Thr
ENST00000643700.1:n.1141G>C
ENST00000643968.1:c.*216G>C	ENSP00000495139.1:n.*216G>C
ENST00000643980.1:n.1357G>C
ENST00000644003.1:c.56G>C	ENSP00000495387.1:p.Arg19Thr
ENST00000644170.1:n.631G>C
ENST00000644177.1:c.362G>C	ENSP00000495079.1:p.Arg121Thr
ENST00000644448.1:n.964G>C
ENST00000644710.1:c.413G>C	ENSP00000493791.1:p.Arg138Thr
ENST00000644885.1:c.426+1956G>C	ENSP00000496146.1:n.426+1956G>C
ENST00000645234.1:c.464G>C	ENSP00000494288.1:p.Arg155Thr
ENST00000645249.1:c.*537G>C	ENSP00000496152.1:n.*537G>C
ENST00000645260.1:c.353G>C	ENSP00000493931.1:p.Arg118Thr
ENST00000645623.1:c.464G>C	ENSP00000495998.1:p.Arg155Thr
ENST00000645768.1:n.1091G>C
ENST00000645840.1:c.*282G>C	ENSP00000494445.1:n.*282G>C
ENST00000645910.1:c.*216G>C	ENSP00000493697.1:n.*216G>C
ENST00000646305.1:c.464G>C	ENSP00000495902.1:p.Arg155Thr
ENST00000646477.1:c.56G>C	ENSP00000495439.1:p.Arg19Thr
ENST00000646561.1:c.464G>C	ENSP00000496569.1:p.Arg155Thr
ENST00000646814.1:c.464G>C	ENSP00000495422.1:p.Arg155Thr
ENST00000647026.1:c.464G>C	ENSP00000494370.1:p.Arg155Thr
ENST00000647155.1:n.629G>C
ENST00000647348.1:c.464G>C	ENSP00000495912.1:p.Arg155Thr
ENST00000217244.7:c.464G>C	ENSP00000217244.3:p.Arg155Thr
ENST00000349736.9:c.464G>C	ENSP00000339247.5:p.Arg155Thr
ENST00000400217.6:c.56G>C	ENSP00000383076.1:p.Arg19Thr
ENST00000400227.7:c.464G>C	ENSP00000383086.3:p.Arg155Thr
ENST00000460062.6:c.56G>C	ENSP00000477147.1:p.Arg19Thr
ENST00000619188.4:c.464G>C	ENSP00000479630.1:p.Arg155Thr
NM_001895.3:c.464G>C	NP_001886.1:p.Arg155Thr
NM_177559.2:c.464G>C	NP_808227.1:p.Arg155Thr
NM_177560.2:c.56G>C	NP_808228.1:p.Arg19Thr
XM_011529175.1:c.464G>C	XP_011527477.1:p.Arg155Thr
XM_011529176.1:c.56G>C	XP_011527478.1:p.Arg19Thr
NM_001362770.1:c.464G>C	NP_001349699.1:p.Arg155Thr
NM_001362771.1:c.464G>C	NP_001349700.1:p.Arg155Thr
NM_177559.3:c.464G>C MANE Select	NP_808227.1:p.Arg155Thr
NM_001362770.2:c.464G>C	NP_001349699.1:p.Arg155Thr
NM_001362771.2:c.464G>C	NP_001349700.1:p.Arg155Thr
NM_001895.4:c.464G>C	NP_001886.1:p.Arg155Thr
NM_177560.3:c.56G>C	NP_808228.1:p.Arg19Thr