Canonical Allele Identifier: CA977778580

Gene: CSNK2A2

Linked Data

• dbSNP Id: rs1961852049
• gnomAD v3: 16-58175424-TGAAA-T
• gnomAD v4: 16-58175424-TGAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58175427_58175430del , CM000678.2:g.58175427_58175430del	GRCh38
NC_000016.9:g.58209331_58209334del , CM000678.1:g.58209331_58209334del	GRCh37
NC_000016.8:g.56766832_56766835del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262506.8:c.370-918_370-915del MANE Select	ENSP00000262506.3:n.370-918_370-915del
ENST00000563307.2:n.2179-918_2179-915del
ENST00000565188.2:c.217-918_217-915del	ENSP00000454874.2:n.217-918_217-915del
ENST00000677823.1:n.2179-918_2179-915del
ENST00000262506.7:c.370-918_370-915del	ENSP00000262506.3:n.370-918_370-915del
ENST00000562367.1:n.195-918_195-915del
ENST00000565188.1:c.370-918_370-915del	ENSP00000454874.1:n.370-918_370-915del
ENST00000566813.5:n.422-918_422-915del
ENST00000567730.6:c.154-7633_154-7630del	ENSP00000456606.2:n.154-7633_154-7630del
NM_001896.2:c.370-918_370-915del	NP_001887.1:n.370-918_370-915del
XM_005255800.2:c.217-918_217-915del	XP_005255857.1:n.217-918_217-915del
XM_005255801.2:c.-42-918_-42-915del	XP_005255858.1:n.-42-918_-42-915del
NM_001896.3:c.370-918_370-915del	NP_001887.1:n.370-918_370-915del
XM_005255800.4:c.217-918_217-915del	XP_005255857.1:n.217-918_217-915del
XM_005255801.3:c.-42-918_-42-915del	XP_005255858.1:n.-42-918_-42-915del
NM_001896.4:c.370-918_370-915del MANE Select	NP_001887.1:n.370-918_370-915del