Canonical Allele Identifier: CA509340282

Gene: CSNK2A1

Linked Data

• MyVariant Identifiers: chr20:g.476438A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.495794A>G , CM000682.2:g.495794A>G	GRCh38
NC_000020.10:g.476438A>G , CM000682.1:g.476438A>G	GRCh37
NC_000020.9:g.424438A>G	NCBI36
NG_011970.1:g.53045T>C
NG_011970.2:g.53045T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217244.9:c.435T>C MANE Select	ENSP00000217244.3:p.Asp145=
ENST00000349736.10:c.27T>C	ENSP00000339247.6:p.Asp9=
ENST00000400217.7:c.435T>C	ENSP00000383076.2:p.Asp145=
ENST00000400227.8:c.435T>C	ENSP00000383086.3:p.Asp145=
ENST00000460062.7:c.27T>C	ENSP00000477147.2:p.Asp9=
ENST00000642689.1:c.384T>C	ENSP00000495414.1:p.Asp128=
ENST00000643600.1:c.435T>C	ENSP00000494038.1:p.Asp145=
ENST00000643602.1:n.454T>C
ENST00000643641.1:n.485T>C
ENST00000643660.1:c.435T>C	ENSP00000495248.1:p.Asp145=
ENST00000643680.1:c.435T>C	ENSP00000493704.1:p.Asp145=
ENST00000643700.1:n.1112T>C
ENST00000643968.1:c.*187T>C	ENSP00000495139.1:n.*187T>C
ENST00000643980.1:n.1328T>C
ENST00000644003.1:c.27T>C	ENSP00000495387.1:p.Asp9=
ENST00000644170.1:n.602T>C
ENST00000644177.1:c.333T>C	ENSP00000495079.1:p.Asp111=
ENST00000644448.1:n.935T>C
ENST00000644710.1:c.384T>C	ENSP00000493791.1:p.Asp128=
ENST00000644885.1:c.426+1927T>C	ENSP00000496146.1:n.426+1927T>C
ENST00000645234.1:c.435T>C	ENSP00000494288.1:p.Asp145=
ENST00000645249.1:c.*508T>C	ENSP00000496152.1:n.*508T>C
ENST00000645260.1:c.324T>C	ENSP00000493931.1:p.Asp108=
ENST00000645623.1:c.435T>C	ENSP00000495998.1:p.Asp145=
ENST00000645768.1:n.1062T>C
ENST00000645840.1:c.*253T>C	ENSP00000494445.1:n.*253T>C
ENST00000645910.1:c.*187T>C	ENSP00000493697.1:n.*187T>C
ENST00000646305.1:c.435T>C	ENSP00000495902.1:p.Asp145=
ENST00000646477.1:c.27T>C	ENSP00000495439.1:p.Asp9=
ENST00000646561.1:c.435T>C	ENSP00000496569.1:p.Asp145=
ENST00000646814.1:c.435T>C	ENSP00000495422.1:p.Asp145=
ENST00000647026.1:c.435T>C	ENSP00000494370.1:p.Asp145=
ENST00000647155.1:n.600T>C
ENST00000647348.1:c.435T>C	ENSP00000495912.1:p.Asp145=
ENST00000217244.7:c.435T>C	ENSP00000217244.3:p.Asp145=
ENST00000349736.9:c.435T>C	ENSP00000339247.5:p.Asp145=
ENST00000400217.6:c.27T>C	ENSP00000383076.1:p.Asp9=
ENST00000400227.7:c.435T>C	ENSP00000383086.3:p.Asp145=
ENST00000460062.6:c.27T>C	ENSP00000477147.1:p.Asp9=
ENST00000619188.4:c.435T>C	ENSP00000479630.1:p.Asp145=
NM_001895.3:c.435T>C	NP_001886.1:p.Asp145=
NM_177559.2:c.435T>C	NP_808227.1:p.Asp145=
NM_177560.2:c.27T>C	NP_808228.1:p.Asp9=
XM_011529175.1:c.435T>C	XP_011527477.1:p.Asp145=
XM_011529176.1:c.27T>C	XP_011527478.1:p.Asp9=
NM_001362770.1:c.435T>C	NP_001349699.1:p.Asp145=
NM_001362771.1:c.435T>C	NP_001349700.1:p.Asp145=
NM_177559.3:c.435T>C MANE Select	NP_808227.1:p.Asp145=
NM_001362770.2:c.435T>C	NP_001349699.1:p.Asp145=
NM_001362771.2:c.435T>C	NP_001349700.1:p.Asp145=
NM_001895.4:c.435T>C	NP_001886.1:p.Asp145=
NM_177560.3:c.27T>C	NP_808228.1:p.Asp9=