Canonical Allele Identifier: CA622696223

Gene: CSNK2A2

Linked Data

• dbSNP Id: rs1428115422
• gnomAD v2: 16-58209331-AAG-A
• gnomAD v3: 16-58175427-AAG-A
• gnomAD v4: 16-58175427-AAG-A
• MyVariant Identifiers: chr16:g.58209332_58209333del (hg19) ; chr16:g.58175428_58175429del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58175433_58175434del , CM000678.2:g.58175433_58175434del	GRCh38
NC_000016.9:g.58209337_58209338del , CM000678.1:g.58209337_58209338del	GRCh37
NC_000016.8:g.56766838_56766839del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262506.8:c.370-919_370-918del MANE Select	ENSP00000262506.3:n.370-919_370-918del
ENST00000563307.2:n.2179-919_2179-918del
ENST00000565188.2:c.217-919_217-918del	ENSP00000454874.2:n.217-919_217-918del
ENST00000677823.1:n.2179-919_2179-918del
ENST00000262506.7:c.370-919_370-918del	ENSP00000262506.3:n.370-919_370-918del
ENST00000562367.1:n.195-919_195-918del
ENST00000565188.1:c.370-919_370-918del	ENSP00000454874.1:n.370-919_370-918del
ENST00000566813.5:n.422-919_422-918del
ENST00000567730.6:c.154-7634_154-7633del	ENSP00000456606.2:n.154-7634_154-7633del
NM_001896.2:c.370-919_370-918del	NP_001887.1:n.370-919_370-918del
XM_005255800.2:c.217-919_217-918del	XP_005255857.1:n.217-919_217-918del
XM_005255801.2:c.-42-919_-42-918del	XP_005255858.1:n.-42-919_-42-918del
NM_001896.3:c.370-919_370-918del	NP_001887.1:n.370-919_370-918del
XM_005255800.4:c.217-919_217-918del	XP_005255857.1:n.217-919_217-918del
XM_005255801.3:c.-42-919_-42-918del	XP_005255858.1:n.-42-919_-42-918del
NM_001896.4:c.370-919_370-918del MANE Select	NP_001887.1:n.370-919_370-918del