Canonical Allele Identifier: CA2678013774

Gene: CSNK2B

Linked Data

• gnomAD v4: 6-31667969-T-TCACCAGGCTCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31667969_31667970insCACCAGGCTCCA , CM000668.2:g.31667969_31667970insCACCAGGCTCCA	GRCh38
NC_000006.11:g.31635746_31635747insCACCAGGCTCCA , CM000668.1:g.31635746_31635747insCACCAGGCTCCA	GRCh37
NC_000006.10:g.31743725_31743726insCACCAGGCTCCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375882.7:c.174_175insCACCAGGCTCCA MANE Select	ENSP00000365042.3:p.Pro58_Asp59insHisGlnAlaPro
ENST00000465481.6:n.307_308insCACCAGGCTCCA
ENST00000475875.2:n.1257_1258insCACCAGGCTCCA
ENST00000677388.1:c.231_232insCACCAGGCTCCA	ENSP00000504290.1:p.Pro77_Val78insHisGlnAlaPro
ENST00000677536.1:c.231_232insCACCAGGCTCCA	ENSP00000502967.1:p.Pro77_Asp78insHisGlnAlaPro
ENST00000677758.1:c.231_232insCACCAGGCTCCA	ENSP00000504242.1:p.Pro77_Asp78insHisGlnAlaPro
ENST00000375865.6:c.174_175insCACCAGGCTCCA	ENSP00000365025.2:p.Pro58_Asp59insHisGlnAlaPro
ENST00000375866.2:c.174_175insCACCAGGCTCCA	ENSP00000365026.2:p.Pro58_Asp59insHisGlnAlaPro
ENST00000375880.6:c.174_175insCACCAGGCTCCA	ENSP00000365040.2:p.Pro58_Asp59insHisGlnAlaPro
ENST00000375882.6:c.174_175insCACCAGGCTCCA	ENSP00000365042.2:p.Pro58_Asp59insHisGlnAlaPro
ENST00000375885.8:c.231_232insCACCAGGCTCCA	ENSP00000365046.4:p.Pro77_Asp78insHisGlnAlaPro
ENST00000465481.5:n.307_308insCACCAGGCTCCA
ENST00000468255.5:n.313_314insCACCAGGCTCCA
ENST00000481269.1:n.300_301insCACCAGGCTCCA
ENST00000617558.2:c.174_175insCACCAGGCTCCA	ENSP00000483989.2:p.Pro58_Asp59insHisGlnAlaPro
NM_001282385.1:c.174_175insCACCAGGCTCCA	NP_001269314.1:p.Pro58_Asp59insHisGlnAlaPro
NM_001320.6:c.174_175insCACCAGGCTCCA	NP_001311.3:p.Pro58_Asp59insHisGlnAlaPro
NM_001320.7:c.174_175insCACCAGGCTCCA MANE Select	NP_001311.3:p.Pro58_Asp59insHisGlnAlaPro
NM_001282385.2:c.174_175insCACCAGGCTCCA	NP_001269314.1:p.Pro58_Asp59insHisGlnAlaPro