Canonical Allele Identifier: CA1979717607

Gene: BBS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515010_66515011delinsGT , CM000673.2:g.66515010_66515011delinsGT	GRCh38
NC_000011.9:g.66282481_66282482delinsGT , CM000673.1:g.66282481_66282482delinsGT	GRCh37
NC_000011.8:g.66039057_66039058delinsGT	NCBI36
NG_009093.1:g.9363_9364delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.432+332_432+333delinsGT MANE Select	ENSP00000317469.7:n.432+332_432+333delinsGT
ENST00000318312.11:c.432+332_432+333delinsGT	ENSP00000317469.7:n.432+332_432+333delinsGT
ENST00000393994.4:c.432+332_432+333delinsGT	ENSP00000377563.2:n.432+332_432+333delinsGT
ENST00000419755.3:c.543+332_543+333delinsGT	ENSP00000398526.3:n.543+332_543+333delinsGT
ENST00000455748.6:c.432+332_432+333delinsGT	ENSP00000405764.2:n.432+332_432+333delinsGT
ENST00000524458.5:c.*139+332_*139+333delinsGT	ENSP00000436195.1:n.*139+332_*139+333delinsGT
ENST00000524705.2:c.153+332_153+333delinsGT	ENSP00000436927.1:n.153+332_153+333delinsGT
ENST00000524907.5:n.422+332_422+333delinsGT
ENST00000525809.5:c.160-530_160-529delinsGT	ENSP00000431187.1:n.160-530_160-529delinsGT
ENST00000526035.5:c.*139+332_*139+333delinsGT	ENSP00000434197.1:n.*139+332_*139+333delinsGT
ENST00000526760.5:c.*139+332_*139+333delinsGT	ENSP00000432140.1:n.*139+332_*139+333delinsGT
ENST00000527251.5:c.*139+332_*139+333delinsGT	ENSP00000434360.1:n.*139+332_*139+333delinsGT
ENST00000529766.5:n.439+332_439+333delinsGT
ENST00000529953.5:n.84+332_84+333delinsGT
ENST00000529955.5:n.450+332_450+333delinsGT
ENST00000532908.5:c.*139+332_*139+333delinsGT	ENSP00000431866.1:n.*139+332_*139+333delinsGT
ENST00000533430.5:n.210+332_210+333delinsGT
ENST00000533557.5:c.*139+332_*139+333delinsGT	ENSP00000434619.1:n.*139+332_*139+333delinsGT
ENST00000533644.5:c.432+332_432+333delinsGT	ENSP00000436073.1:n.432+332_432+333delinsGT
ENST00000534730.5:n.444+332_444+333delinsGT
ENST00000630659.2:c.*139+332_*139+333delinsGT	ENSP00000486455.1:n.*139+332_*139+333delinsGT
NM_024649.4:c.432+332_432+333delinsGT	NP_078925.3:n.432+332_432+333delinsGT
NM_024649.5:c.432+332_432+333delinsGT MANE Select	NP_078925.3:n.432+332_432+333delinsGT