Canonical Allele Identifier: CA407940326
Gene: CSNK2A1 HGNC NCBI

Linked Data

gnomAD v4: 20-505207-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.505207C>G , CM000682.2:g.505207C>G GRCh38
NC_000020.10:g.485851C>G , CM000682.1:g.485851C>G GRCh37
NC_000020.9:g.433851C>G NCBI36
NG_011970.1:g.43632G>C
NG_011970.2:g.43632G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217244.9:c.124G>C MANE Select ENSP00000217244.3:p.Val42Leu
ENST00000349736.10:c.-285G>C ENSP00000339247.6:n.-285G>C
ENST00000400217.7:c.124G>C ENSP00000383076.2:p.Val42Leu
ENST00000400227.8:c.124G>C ENSP00000383086.3:p.Val42Leu
ENST00000460062.7:c.-285G>C ENSP00000477147.2:n.-285G>C
ENST00000608066.6:c.124G>C ENSP00000476486.2:p.Val42Leu
ENST00000609525.2:c.124G>C ENSP00000476547.2:p.Val42Leu
ENST00000609606.6:n.352G>C
ENST00000642160.1:c.124G>C ENSP00000496115.1:p.Val42Leu
ENST00000642689.1:c.124G>C ENSP00000495414.1:p.Val42Leu
ENST00000643600.1:c.124G>C ENSP00000494038.1:p.Val42Leu
ENST00000643660.1:c.124G>C ENSP00000495248.1:p.Val42Leu
ENST00000643680.1:c.124G>C ENSP00000493704.1:p.Val42Leu
ENST00000643700.1:n.274G>C
ENST00000643968.1:c.124G>C ENSP00000495139.1:p.Val42Leu
ENST00000644003.1:c.-391G>C ENSP00000495387.1:n.-391G>C
ENST00000644170.1:n.291G>C
ENST00000644177.1:c.124G>C ENSP00000495079.1:p.Val42Leu
ENST00000644710.1:c.124G>C ENSP00000493791.1:p.Val42Leu
ENST00000644885.1:c.124G>C ENSP00000496146.1:p.Val42Leu
ENST00000645091.1:c.124G>C ENSP00000495942.1:p.Val42Leu
ENST00000645187.1:c.124G>C ENSP00000496232.1:p.Val42Leu
ENST00000645234.1:c.124G>C ENSP00000494288.1:p.Val42Leu
ENST00000645249.1:c.124G>C ENSP00000496152.1:p.Val42Leu
ENST00000645260.1:c.124G>C ENSP00000493931.1:p.Val42Leu
ENST00000645623.1:c.124G>C ENSP00000495998.1:p.Val42Leu
ENST00000645641.1:n.71G>C
ENST00000645840.1:c.124G>C ENSP00000494445.1:p.Val42Leu
ENST00000645910.1:c.124G>C ENSP00000493697.1:p.Val42Leu
ENST00000646305.1:c.124G>C ENSP00000495902.1:p.Val42Leu
ENST00000646443.1:n.29G>C
ENST00000646477.1:c.-419G>C ENSP00000495439.1:n.-419G>C
ENST00000646561.1:c.124G>C ENSP00000496569.1:p.Val42Leu
ENST00000646814.1:c.124G>C ENSP00000495422.1:p.Val42Leu
ENST00000646908.1:c.124G>C ENSP00000493643.1:p.Val42Leu
ENST00000647026.1:c.124G>C ENSP00000494370.1:p.Val42Leu
ENST00000647155.1:n.289G>C
ENST00000647348.1:c.124G>C ENSP00000495912.1:p.Val42Leu
ENST00000217244.7:c.124G>C ENSP00000217244.3:p.Val42Leu
ENST00000349736.9:c.124G>C ENSP00000339247.5:p.Val42Leu
ENST00000400217.6:c.-285G>C ENSP00000383076.1:n.-285G>C
ENST00000400227.7:c.124G>C ENSP00000383086.3:p.Val42Leu
ENST00000460062.6:c.-391G>C ENSP00000477147.1:n.-391G>C
ENST00000608066.5:c.124G>C ENSP00000476486.1:p.Val42Leu
ENST00000608490.1:n.135G>C
ENST00000609525.1:c.124G>C ENSP00000476547.1:p.Val42Leu
ENST00000609606.5:n.291G>C
ENST00000619188.4:c.124G>C ENSP00000479630.1:p.Val42Leu
NM_001895.3:c.124G>C NP_001886.1:p.Val42Leu
NM_177559.2:c.124G>C NP_808227.1:p.Val42Leu
NM_177560.2:c.-285G>C NP_808228.1:n.-285G>C
XM_011529175.1:c.124G>C XP_011527477.1:p.Val42Leu
XM_011529176.1:c.-370G>C XP_011527478.1:n.-370G>C
NM_001362770.1:c.124G>C NP_001349699.1:p.Val42Leu
NM_001362771.1:c.124G>C NP_001349700.1:p.Val42Leu
NM_177559.3:c.124G>C MANE Select NP_808227.1:p.Val42Leu
NM_001362770.2:c.124G>C NP_001349699.1:p.Val42Leu
NM_001362771.2:c.124G>C NP_001349700.1:p.Val42Leu
NM_001895.4:c.124G>C NP_001886.1:p.Val42Leu
NM_177560.3:c.-285G>C NP_808228.1:n.-285G>C