Canonical Allele Identifier: CA3718580

Gene: CSNK2B

Linked Data

• dbSNP Id: rs749877372
• ExAC: 6:31635760 CAG / C
• gnomAD v2: 6-31635760-CAG-C
• gnomAD v4: 6-31667983-CAG-C
• MyVariant Identifiers: chr6:g.31635761_31635762del (hg19) ; chr6:g.31667984_31667985del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31667984_31667985del , CM000668.2:g.31667984_31667985del	GRCh38
NC_000006.11:g.31635761_31635762del , CM000668.1:g.31635761_31635762del	GRCh37
NC_000006.10:g.31743740_31743741del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375882.7:c.175+14_175+15del MANE Select	ENSP00000365042.3:n.175+14_175+15del
ENST00000465481.6:n.322_323del
ENST00000475875.2:n.1272_1273del
ENST00000677388.1:c.232+14_232+15del	ENSP00000504290.1:n.232+14_232+15del
ENST00000677536.1:c.232+14_232+15del	ENSP00000502967.1:n.232+14_232+15del
ENST00000677758.1:c.232+14_232+15del	ENSP00000504242.1:n.232+14_232+15del
ENST00000375865.6:c.175+14_175+15del	ENSP00000365025.2:n.175+14_175+15del
ENST00000375866.2:c.175+14_175+15del	ENSP00000365026.2:n.175+14_175+15del
ENST00000375880.6:c.175+14_175+15del	ENSP00000365040.2:n.175+14_175+15del
ENST00000375882.6:c.175+14_175+15del	ENSP00000365042.2:n.175+14_175+15del
ENST00000375885.8:c.232+14_232+15del	ENSP00000365046.4:n.232+14_232+15del
ENST00000465481.5:n.322_323del
ENST00000468255.5:n.314+14_314+15del
ENST00000481269.1:n.301+14_301+15del
ENST00000617558.2:c.175+14_175+15del	ENSP00000483989.2:n.175+14_175+15del
NM_001282385.1:c.175+14_175+15del	NP_001269314.1:n.175+14_175+15del
NM_001320.6:c.175+14_175+15del	NP_001311.3:n.175+14_175+15del
NM_001320.7:c.175+14_175+15del MANE Select	NP_001311.3:n.175+14_175+15del
NM_001282385.2:c.175+14_175+15del	NP_001269314.1:n.175+14_175+15del