Canonical Allele Identifier: CA915944175

Gene: CSNK2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31669899dup , CM000668.2:g.31669899dup	GRCh38
NC_000006.11:g.31637676dup , CM000668.1:g.31637676dup	GRCh37
NC_000006.10:g.31745655dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001320.7:c.621dup MANE Select	NP_001311.3:p.Lys208GlnfsTer?
ENST00000375882.7:c.621dup MANE Select	ENSP00000365042.3:p.Lys208GlnfsTer?
NM_001282385.1:c.612dup	NP_001269314.1:p.Lys205GlnfsTer?
NM_001282385.2:c.612dup	NP_001269314.1:p.Lys205GlnfsTer?
NM_001320.6:c.621dup	NP_001311.3:p.Lys208GlnfsTer?
ENST00000375865.6:c.621dup	ENSP00000365025.2:p.Lys208GlnfsTer?
ENST00000375866.2:c.621dup	ENSP00000365026.2:p.Lys208GlnfsTer?
ENST00000375880.6:c.557+391dup	ENSP00000365040.2:n.557+391dup
ENST00000375882.6:c.621dup	ENSP00000365042.2:p.Lys208GlnfsTer?
ENST00000375885.8:c.678dup	ENSP00000365046.4:p.Lys227GlnfsTer?
ENST00000409691.1:c.55+727dup	ENSP00000387322.1:n.55+727dup
ENST00000468255.5:n.1348dup
ENST00000475875.2:n.2272dup
ENST00000617558.2:c.367+727dup	ENSP00000483989.2:n.367+727dup
ENST00000677388.1:c.*407dup	ENSP00000504290.1:n.*407dup
ENST00000677536.1:c.669dup	ENSP00000502967.1:p.Lys224GlnfsTer?
ENST00000677758.1:c.*221dup	ENSP00000504242.1:n.*221dup