Canonical Allele Identifier: CA9723957

Gene: CSNK2A1

Linked Data

• dbSNP Id: rs761701003
• ExAC: 20:476349 GC / G
• gnomAD v2: 20-476349-GC-G
• gnomAD v4: 20-495705-GC-G
• MyVariant Identifiers: chr20:g.476350del (hg19) ; chr20:g.495707del (hg38) ; chr20:g.495706del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.495707del , CM000682.2:g.495707del	GRCh38
NC_000020.10:g.476351del , CM000682.1:g.476351del	GRCh37
NC_000020.9:g.424351del	NCBI36
NG_011970.1:g.53133del
NG_011970.2:g.53133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217244.9:c.510+13del MANE Select	ENSP00000217244.3:n.510+13del
ENST00000349736.10:c.102+13del	ENSP00000339247.6:n.102+13del
ENST00000400217.7:c.510+13del	ENSP00000383076.2:n.510+13del
ENST00000400227.8:c.510+13del	ENSP00000383086.3:n.510+13del
ENST00000460062.7:c.102+13del	ENSP00000477147.2:n.102+13del
ENST00000642689.1:c.459+13del	ENSP00000495414.1:n.459+13del
ENST00000643600.1:c.510+13del	ENSP00000494038.1:n.510+13del
ENST00000643602.1:n.542del
ENST00000643641.1:n.560+13del
ENST00000643660.1:c.510+13del	ENSP00000495248.1:n.510+13del
ENST00000643680.1:c.510+13del	ENSP00000493704.1:n.510+13del
ENST00000643700.1:n.1187+13del
ENST00000643968.1:c.*275del	ENSP00000495139.1:n.*275del
ENST00000643980.1:n.1403+13del
ENST00000644003.1:c.102+13del	ENSP00000495387.1:n.102+13del
ENST00000644170.1:n.677+13del
ENST00000644448.1:n.1010+13del
ENST00000644710.1:c.459+13del	ENSP00000493791.1:n.459+13del
ENST00000644885.1:c.426+2015del	ENSP00000496146.1:n.426+2015del
ENST00000645234.1:c.510+13del	ENSP00000494288.1:n.510+13del
ENST00000645249.1:c.*583+13del	ENSP00000496152.1:n.*583+13del
ENST00000645260.1:c.399+13del	ENSP00000493931.1:n.399+13del
ENST00000645623.1:c.510+13del	ENSP00000495998.1:n.510+13del
ENST00000645768.1:n.1137+13del
ENST00000645840.1:c.*328+13del	ENSP00000494445.1:n.*328+13del
ENST00000645910.1:c.*262+13del	ENSP00000493697.1:n.*262+13del
ENST00000646305.1:c.510+13del	ENSP00000495902.1:n.510+13del
ENST00000646477.1:c.102+13del	ENSP00000495439.1:n.102+13del
ENST00000646561.1:c.510+13del	ENSP00000496569.1:n.510+13del
ENST00000646814.1:c.510+13del	ENSP00000495422.1:n.510+13del
ENST00000647026.1:c.510+13del	ENSP00000494370.1:n.510+13del
ENST00000647155.1:n.675+13del
ENST00000647348.1:c.510+13del	ENSP00000495912.1:n.510+13del
ENST00000217244.7:c.510+13del	ENSP00000217244.3:n.510+13del
ENST00000349736.9:c.510+13del	ENSP00000339247.5:n.510+13del
ENST00000400217.6:c.102+13del	ENSP00000383076.1:n.102+13del
ENST00000400227.7:c.510+13del	ENSP00000383086.3:n.510+13del
ENST00000619188.4:c.510+13del	ENSP00000479630.1:n.510+13del
NM_001895.3:c.510+13del	NP_001886.1:n.510+13del
NM_177559.2:c.510+13del	NP_808227.1:n.510+13del
NM_177560.2:c.102+13del	NP_808228.1:n.102+13del
XM_011529175.1:c.510+13del	XP_011527477.1:n.510+13del
XM_011529176.1:c.102+13del	XP_011527478.1:n.102+13del
NM_001362770.1:c.510+13del	NP_001349699.1:n.510+13del
NM_001362771.1:c.510+13del	NP_001349700.1:n.510+13del
NM_177559.3:c.510+13del MANE Select	NP_808227.1:n.510+13del
NM_001362770.2:c.510+13del	NP_001349699.1:n.510+13del
NM_001362771.2:c.510+13del	NP_001349700.1:n.510+13del
NM_001895.4:c.510+13del	NP_001886.1:n.510+13del
NM_177560.3:c.102+13del	NP_808228.1:n.102+13del