Canonical Allele Identifier: CA2651536314

Gene: CSNK2A1

Linked Data

• gnomAD v4: 20-505095-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.505095C>T , CM000682.2:g.505095C>T	GRCh38
NC_000020.10:g.485739C>T , CM000682.1:g.485739C>T	GRCh37
NC_000020.9:g.433739C>T	NCBI36
NG_011970.1:g.43744G>A
NG_011970.2:g.43744G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217244.9:c.213+23G>A MANE Select	ENSP00000217244.3:n.213+23G>A
ENST00000349736.10:c.-196+23G>A	ENSP00000339247.6:n.-196+23G>A
ENST00000400217.7:c.213+23G>A	ENSP00000383076.2:n.213+23G>A
ENST00000400227.8:c.213+23G>A	ENSP00000383086.3:n.213+23G>A
ENST00000460062.7:c.-196+23G>A	ENSP00000477147.2:n.-196+23G>A
ENST00000608066.6:c.213+23G>A	ENSP00000476486.2:n.213+23G>A
ENST00000609525.2:c.213+23G>A	ENSP00000476547.2:n.213+23G>A
ENST00000609606.6:n.441+23G>A
ENST00000642160.1:c.236G>A	ENSP00000496115.1:p.Arg79Lys
ENST00000642689.1:c.213+23G>A	ENSP00000495414.1:n.213+23G>A
ENST00000643600.1:c.213+23G>A	ENSP00000494038.1:n.213+23G>A
ENST00000643660.1:c.213+23G>A	ENSP00000495248.1:n.213+23G>A
ENST00000643680.1:c.213+23G>A	ENSP00000493704.1:n.213+23G>A
ENST00000643700.1:n.363+23G>A
ENST00000643968.1:c.213+23G>A	ENSP00000495139.1:n.213+23G>A
ENST00000644003.1:c.-302+23G>A	ENSP00000495387.1:n.-302+23G>A
ENST00000644170.1:n.380+23G>A
ENST00000644177.1:c.213+23G>A	ENSP00000495079.1:n.213+23G>A
ENST00000644710.1:c.213+23G>A	ENSP00000493791.1:n.213+23G>A
ENST00000644885.1:c.213+23G>A	ENSP00000496146.1:n.213+23G>A
ENST00000645091.1:c.213+23G>A	ENSP00000495942.1:n.213+23G>A
ENST00000645187.1:c.213+23G>A	ENSP00000496232.1:n.213+23G>A
ENST00000645234.1:c.213+23G>A	ENSP00000494288.1:n.213+23G>A
ENST00000645249.1:c.213+23G>A	ENSP00000496152.1:n.213+23G>A
ENST00000645260.1:c.213+23G>A	ENSP00000493931.1:n.213+23G>A
ENST00000645623.1:c.213+23G>A	ENSP00000495998.1:n.213+23G>A
ENST00000645641.1:n.160+23G>A
ENST00000645840.1:c.213+23G>A	ENSP00000494445.1:n.213+23G>A
ENST00000645910.1:c.213+23G>A	ENSP00000493697.1:n.213+23G>A
ENST00000646305.1:c.213+23G>A	ENSP00000495902.1:n.213+23G>A
ENST00000646443.1:n.118+23G>A
ENST00000646477.1:c.-330+23G>A	ENSP00000495439.1:n.-330+23G>A
ENST00000646561.1:c.213+23G>A	ENSP00000496569.1:n.213+23G>A
ENST00000646814.1:c.213+23G>A	ENSP00000495422.1:n.213+23G>A
ENST00000646908.1:c.213+23G>A	ENSP00000493643.1:n.213+23G>A
ENST00000647026.1:c.213+23G>A	ENSP00000494370.1:n.213+23G>A
ENST00000647155.1:n.378+23G>A
ENST00000647348.1:c.213+23G>A	ENSP00000495912.1:n.213+23G>A
ENST00000217244.7:c.213+23G>A	ENSP00000217244.3:n.213+23G>A
ENST00000349736.9:c.213+23G>A	ENSP00000339247.5:n.213+23G>A
ENST00000400217.6:c.-196+23G>A	ENSP00000383076.1:n.-196+23G>A
ENST00000400227.7:c.213+23G>A	ENSP00000383086.3:n.213+23G>A
ENST00000460062.6:c.-302+23G>A	ENSP00000477147.1:n.-302+23G>A
ENST00000608066.5:c.213+23G>A	ENSP00000476486.1:n.213+23G>A
ENST00000608490.1:n.247G>A
ENST00000609525.1:c.213+23G>A	ENSP00000476547.1:n.213+23G>A
ENST00000609606.5:n.380+23G>A
ENST00000619188.4:c.213+23G>A	ENSP00000479630.1:n.213+23G>A
NM_001895.3:c.213+23G>A	NP_001886.1:n.213+23G>A
NM_177559.2:c.213+23G>A	NP_808227.1:n.213+23G>A
NM_177560.2:c.-196+23G>A	NP_808228.1:n.-196+23G>A
XM_011529175.1:c.213+23G>A	XP_011527477.1:n.213+23G>A
XM_011529176.1:c.-281+23G>A	XP_011527478.1:n.-281+23G>A
NM_001362770.1:c.213+23G>A	NP_001349699.1:n.213+23G>A
NM_001362771.1:c.213+23G>A	NP_001349700.1:n.213+23G>A
NM_177559.3:c.213+23G>A MANE Select	NP_808227.1:n.213+23G>A
NM_001362770.2:c.213+23G>A	NP_001349699.1:n.213+23G>A
NM_001362771.2:c.213+23G>A	NP_001349700.1:n.213+23G>A
NM_001895.4:c.213+23G>A	NP_001886.1:n.213+23G>A
NM_177560.3:c.-196+23G>A	NP_808228.1:n.-196+23G>A