Canonical Allele Identifier: CA915944173
Community Standard Title: NM_001320.7(CSNK2B):c.265del (p.Thr90ProfsTer?)
Gene: CSNK2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31668628del , CM000668.2:g.31668628del GRCh38
NC_000006.11:g.31636405del , CM000668.1:g.31636405del GRCh37
NC_000006.10:g.31744384del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001320.7:c.265del MANE Select NP_001311.3:p.Thr90ProfsTer?
ENST00000375882.7:c.265del MANE Select ENSP00000365042.3:p.Thr90ProfsTer?
NM_001282385.1:c.265del NP_001269314.1:p.Thr90ProfsTer?
NM_001282385.2:c.265del NP_001269314.1:p.Thr90ProfsTer?
NM_001320.6:c.265del NP_001311.3:p.Thr90ProfsTer?
ENST00000375865.6:c.265del ENSP00000365025.2:p.Thr90ProfsTer?
ENST00000375866.2:c.265del ENSP00000365026.2:p.Thr90ProfsTer?
ENST00000375880.6:c.265del ENSP00000365040.2:p.Thr90ProfsTer?
ENST00000375882.6:c.265del ENSP00000365042.2:p.Thr90ProfsTer?
ENST00000375885.8:c.322del ENSP00000365046.4:p.Thr109ProfsTer?
ENST00000465481.6:n.966del
ENST00000468255.5:n.404del
ENST00000475875.2:n.1916del
ENST00000481269.1:n.391del
ENST00000617558.2:c.265del ENSP00000483989.2:p.Thr90ProfsTer?
ENST00000677388.1:c.*51del ENSP00000504290.1:n.*51del
ENST00000677536.1:c.322del ENSP00000502967.1:p.Thr109ProfsTer?
ENST00000677758.1:c.322del ENSP00000504242.1:p.Thr109ProfsTer9