Canonical Allele Identifier: CA363474981

Gene: CSNK2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31669137G>C , CM000668.2:g.31669137G>C	GRCh38
NC_000006.11:g.31636914G>C , CM000668.1:g.31636914G>C	GRCh37
NC_000006.10:g.31744893G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001320.7:c.332G>C MANE Select	NP_001311.3:p.Arg111Pro
ENST00000375882.7:c.332G>C MANE Select	ENSP00000365042.3:p.Arg111Pro
NM_001282385.1:c.332G>C	NP_001269314.1:p.Arg111Pro
NM_001282385.2:c.332G>C	NP_001269314.1:p.Arg111Pro
NM_001320.6:c.332G>C	NP_001311.3:p.Arg111Pro
ENST00000375865.6:c.332G>C	ENSP00000365025.2:p.Arg111Pro
ENST00000375866.2:c.332G>C	ENSP00000365026.2:p.Arg111Pro
ENST00000375880.6:c.332G>C	ENSP00000365040.2:p.Arg111Pro
ENST00000375882.6:c.332G>C	ENSP00000365042.2:p.Arg111Pro
ENST00000375885.8:c.389G>C	ENSP00000365046.4:p.Arg130Pro
ENST00000409691.1:c.20G>C	ENSP00000387322.1:p.Arg7Pro
ENST00000468255.5:n.913G>C
ENST00000475875.2:n.1983G>C
ENST00000481269.1:n.458G>C
ENST00000617558.2:c.332G>C	ENSP00000483989.2:p.Arg111Pro
ENST00000677388.1:c.*118G>C	ENSP00000504290.1:n.*118G>C
ENST00000677536.1:c.389G>C	ENSP00000502967.1:p.Arg130Pro
ENST00000677758.1:c.427G>C	ENSP00000504242.1:p.Val143Leu