Canonical Allele Identifier: CA407932755

Gene: CSNK2A1

Linked Data

• MyVariant Identifiers: chr20:g.476362C>G (hg19) ; chr20:g.495718C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.495718C>G , CM000682.2:g.495718C>G	GRCh38
NC_000020.10:g.476362C>G , CM000682.1:g.476362C>G	GRCh37
NC_000020.9:g.424362C>G	NCBI36
NG_011970.1:g.53121G>C
NG_011970.2:g.53121G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217244.9:c.510+1G>C MANE Select	ENSP00000217244.3:n.510+1G>C
ENST00000349736.10:c.102+1G>C	ENSP00000339247.6:n.102+1G>C
ENST00000400217.7:c.510+1G>C	ENSP00000383076.2:n.510+1G>C
ENST00000400227.8:c.510+1G>C	ENSP00000383086.3:n.510+1G>C
ENST00000460062.7:c.102+1G>C	ENSP00000477147.2:n.102+1G>C
ENST00000642689.1:c.459+1G>C	ENSP00000495414.1:n.459+1G>C
ENST00000643600.1:c.510+1G>C	ENSP00000494038.1:n.510+1G>C
ENST00000643602.1:n.530G>C
ENST00000643641.1:n.560+1G>C
ENST00000643660.1:c.510+1G>C	ENSP00000495248.1:n.510+1G>C
ENST00000643680.1:c.510+1G>C	ENSP00000493704.1:n.510+1G>C
ENST00000643700.1:n.1187+1G>C
ENST00000643968.1:c.*263G>C	ENSP00000495139.1:n.*263G>C
ENST00000643980.1:n.1403+1G>C
ENST00000644003.1:c.102+1G>C	ENSP00000495387.1:n.102+1G>C
ENST00000644170.1:n.677+1G>C
ENST00000644448.1:n.1010+1G>C
ENST00000644710.1:c.459+1G>C	ENSP00000493791.1:n.459+1G>C
ENST00000644885.1:c.426+2003G>C	ENSP00000496146.1:n.426+2003G>C
ENST00000645234.1:c.510+1G>C	ENSP00000494288.1:n.510+1G>C
ENST00000645249.1:c.*583+1G>C	ENSP00000496152.1:n.*583+1G>C
ENST00000645260.1:c.399+1G>C	ENSP00000493931.1:n.399+1G>C
ENST00000645623.1:c.510+1G>C	ENSP00000495998.1:n.510+1G>C
ENST00000645768.1:n.1137+1G>C
ENST00000645840.1:c.*328+1G>C	ENSP00000494445.1:n.*328+1G>C
ENST00000645910.1:c.*262+1G>C	ENSP00000493697.1:n.*262+1G>C
ENST00000646305.1:c.510+1G>C	ENSP00000495902.1:n.510+1G>C
ENST00000646477.1:c.102+1G>C	ENSP00000495439.1:n.102+1G>C
ENST00000646561.1:c.510+1G>C	ENSP00000496569.1:n.510+1G>C
ENST00000646814.1:c.510+1G>C	ENSP00000495422.1:n.510+1G>C
ENST00000647026.1:c.510+1G>C	ENSP00000494370.1:n.510+1G>C
ENST00000647155.1:n.675+1G>C
ENST00000647348.1:c.510+1G>C	ENSP00000495912.1:n.510+1G>C
ENST00000217244.7:c.510+1G>C	ENSP00000217244.3:n.510+1G>C
ENST00000349736.9:c.510+1G>C	ENSP00000339247.5:n.510+1G>C
ENST00000400217.6:c.102+1G>C	ENSP00000383076.1:n.102+1G>C
ENST00000400227.7:c.510+1G>C	ENSP00000383086.3:n.510+1G>C
ENST00000619188.4:c.510+1G>C	ENSP00000479630.1:n.510+1G>C
NM_001895.3:c.510+1G>C	NP_001886.1:n.510+1G>C
NM_177559.2:c.510+1G>C	NP_808227.1:n.510+1G>C
NM_177560.2:c.102+1G>C	NP_808228.1:n.102+1G>C
XM_011529175.1:c.510+1G>C	XP_011527477.1:n.510+1G>C
XM_011529176.1:c.102+1G>C	XP_011527478.1:n.102+1G>C
NM_001362770.1:c.510+1G>C	NP_001349699.1:n.510+1G>C
NM_001362771.1:c.510+1G>C	NP_001349700.1:n.510+1G>C
NM_177559.3:c.510+1G>C MANE Select	NP_808227.1:n.510+1G>C
NM_001362770.2:c.510+1G>C	NP_001349699.1:n.510+1G>C
NM_001362771.2:c.510+1G>C	NP_001349700.1:n.510+1G>C
NM_001895.4:c.510+1G>C	NP_001886.1:n.510+1G>C
NM_177560.3:c.102+1G>C	NP_808228.1:n.102+1G>C