Canonical Allele Identifier: CA363479393

Gene: CSNK2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31669838T>C , CM000668.2:g.31669838T>C	GRCh38
NC_000006.11:g.31637615T>C , CM000668.1:g.31637615T>C	GRCh37
NC_000006.10:g.31745594T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001320.7:c.560T>C MANE Select	NP_001311.3:p.Leu187Pro
ENST00000375882.7:c.560T>C MANE Select	ENSP00000365042.3:p.Leu187Pro
NM_001282385.1:c.551T>C	NP_001269314.1:p.Leu184Pro
NM_001282385.2:c.551T>C	NP_001269314.1:p.Leu184Pro
NM_001320.6:c.560T>C	NP_001311.3:p.Leu187Pro
ENST00000375865.6:c.560T>C	ENSP00000365025.2:p.Leu187Pro
ENST00000375866.2:c.560T>C	ENSP00000365026.2:p.Leu187Pro
ENST00000375880.6:c.557+330T>C	ENSP00000365040.2:n.557+330T>C
ENST00000375882.6:c.560T>C	ENSP00000365042.2:p.Leu187Pro
ENST00000375885.8:c.617T>C	ENSP00000365046.4:p.Leu206Pro
ENST00000409691.1:c.55+666T>C	ENSP00000387322.1:n.55+666T>C
ENST00000468255.5:n.1287T>C
ENST00000475875.2:n.2211T>C
ENST00000617558.2:c.367+666T>C	ENSP00000483989.2:n.367+666T>C
ENST00000677388.1:c.*346T>C	ENSP00000504290.1:n.*346T>C
ENST00000677536.1:c.608T>C	ENSP00000502967.1:p.Leu203Pro
ENST00000677758.1:c.*160T>C	ENSP00000504242.1:n.*160T>C