Canonical Allele Identifier: CA358408

Gene: CSNK2A1

Linked Data

• ClinVar Variation Id: 224797
• ClinVar RCV Id: RCV000239569
• dbSNP Id: rs869312846
• MyVariant Identifiers: chr20:g.469320A>G (hg19) ; chr20:g.488676A>G (hg38)
• PubMed: PMID:27048600

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.488676A>G , CM000682.2:g.488676A>G	GRCh38
NC_000020.10:g.469320A>G , CM000682.1:g.469320A>G	GRCh37
NC_000020.9:g.417320A>G	NCBI36
NG_011970.1:g.60163T>C
NG_011970.2:g.60163T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217244.9:c.824+2T>C MANE Select	ENSP00000217244.3:n.824+2T>C
ENST00000349736.10:c.416+2T>C	ENSP00000339247.6:n.416+2T>C
ENST00000400217.7:c.824+2T>C	ENSP00000383076.2:n.824+2T>C
ENST00000400227.8:c.824+2T>C	ENSP00000383086.3:n.824+2T>C
ENST00000619801.5:c.59+2T>C	ENSP00000481572.1:n.59+2T>C
ENST00000642673.1:n.570+2T>C
ENST00000642689.1:c.773+2T>C	ENSP00000495414.1:n.773+2T>C
ENST00000643641.1:n.874+2T>C
ENST00000643660.1:c.824+2T>C	ENSP00000495248.1:n.824+2T>C
ENST00000643700.1:n.1501+2T>C
ENST00000643980.1:n.1717+2T>C
ENST00000644003.1:c.416+2T>C	ENSP00000495387.1:n.416+2T>C
ENST00000644170.1:n.991+2T>C
ENST00000644448.1:n.1324+2T>C
ENST00000644710.1:c.773+2T>C	ENSP00000493791.1:n.773+2T>C
ENST00000644885.1:c.740+2T>C	ENSP00000496146.1:n.740+2T>C
ENST00000645234.1:c.824+2T>C	ENSP00000494288.1:n.824+2T>C
ENST00000645249.1:c.*897+2T>C	ENSP00000496152.1:n.*897+2T>C
ENST00000645260.1:c.713+2T>C	ENSP00000493931.1:n.713+2T>C
ENST00000645334.1:n.667+2T>C
ENST00000645623.1:c.824+2T>C	ENSP00000495998.1:n.824+2T>C
ENST00000645768.1:n.1451+2T>C
ENST00000645840.1:c.*642+2T>C	ENSP00000494445.1:n.*642+2T>C
ENST00000645910.1:c.*576+2T>C	ENSP00000493697.1:n.*576+2T>C
ENST00000646305.1:c.824+2T>C	ENSP00000495902.1:n.824+2T>C
ENST00000646477.1:c.416+2T>C	ENSP00000495439.1:n.416+2T>C
ENST00000646561.1:c.824+2T>C	ENSP00000496569.1:n.824+2T>C
ENST00000646814.1:c.824+2T>C	ENSP00000495422.1:n.824+2T>C
ENST00000647026.1:c.713+2T>C	ENSP00000494370.1:n.713+2T>C
ENST00000647155.1:n.991T>C
ENST00000647348.1:c.824+2T>C	ENSP00000495912.1:n.824+2T>C
ENST00000217244.7:c.824+2T>C	ENSP00000217244.3:n.824+2T>C
ENST00000349736.9:c.824+2T>C	ENSP00000339247.5:n.824+2T>C
ENST00000400217.6:c.416+2T>C	ENSP00000383076.1:n.416+2T>C
ENST00000400227.7:c.824+2T>C	ENSP00000383086.3:n.824+2T>C
ENST00000619188.4:c.824+2T>C	ENSP00000479630.1:n.824+2T>C
ENST00000619801.4:c.59+2T>C	ENSP00000481572.1:n.59+2T>C
NM_001895.3:c.824+2T>C	NP_001886.1:n.824+2T>C
NM_177559.2:c.824+2T>C	NP_808227.1:n.824+2T>C
NM_177560.2:c.416+2T>C	NP_808228.1:n.416+2T>C
XM_011529175.1:c.824+2T>C	XP_011527477.1:n.824+2T>C
XM_011529176.1:c.416+2T>C	XP_011527478.1:n.416+2T>C
NM_001362770.1:c.824+2T>C	NP_001349699.1:n.824+2T>C
NM_001362771.1:c.824+2T>C	NP_001349700.1:n.824+2T>C
NM_177559.3:c.824+2T>C MANE Select	NP_808227.1:n.824+2T>C
NM_001362770.2:c.824+2T>C	NP_001349699.1:n.824+2T>C
NM_001362771.2:c.824+2T>C	NP_001349700.1:n.824+2T>C
NM_001895.4:c.824+2T>C	NP_001886.1:n.824+2T>C
NM_177560.3:c.416+2T>C	NP_808228.1:n.416+2T>C