Canonical Allele Identifier: CA363473413

Gene: CSNK2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31668619C>T , CM000668.2:g.31668619C>T	GRCh38
NC_000006.11:g.31636396C>T , CM000668.1:g.31636396C>T	GRCh37
NC_000006.10:g.31744375C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001320.7:c.256C>T MANE Select	NP_001311.3:p.Arg86Cys
ENST00000375882.7:c.256C>T MANE Select	ENSP00000365042.3:p.Arg86Cys
NM_001282385.1:c.256C>T	NP_001269314.1:p.Arg86Cys
NM_001282385.2:c.256C>T	NP_001269314.1:p.Arg86Cys
NM_001320.6:c.256C>T	NP_001311.3:p.Arg86Cys
ENST00000375865.6:c.256C>T	ENSP00000365025.2:p.Arg86Cys
ENST00000375866.2:c.256C>T	ENSP00000365026.2:p.Arg86Cys
ENST00000375880.6:c.256C>T	ENSP00000365040.2:p.Arg86Cys
ENST00000375882.6:c.256C>T	ENSP00000365042.2:p.Arg86Cys
ENST00000375885.8:c.313C>T	ENSP00000365046.4:p.Arg105Cys
ENST00000465481.6:n.957C>T
ENST00000468255.5:n.395C>T
ENST00000475875.2:n.1907C>T
ENST00000481269.1:n.382C>T
ENST00000617558.2:c.256C>T	ENSP00000483989.2:p.Arg86Cys
ENST00000677388.1:c.*42C>T	ENSP00000504290.1:n.*42C>T
ENST00000677536.1:c.313C>T	ENSP00000502967.1:p.Arg105Cys
ENST00000677758.1:c.313C>T	ENSP00000504242.1:p.Arg105Cys