Canonical Allele Identifier: CA2792478577

Gene: BBS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514896_66514897insAGAT , CM000673.2:g.66514896_66514897insAGAT	GRCh38
NC_000011.9:g.66282367_66282368insAGAT , CM000673.1:g.66282367_66282368insAGAT	GRCh37
NC_000011.8:g.66038943_66038944insAGAT	NCBI36
NG_009093.1:g.9249_9250insAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.432+218_432+219insAGAT MANE Select	ENSP00000317469.7:n.432+218_432+219insAGAT
ENST00000318312.11:c.432+218_432+219insAGAT	ENSP00000317469.7:n.432+218_432+219insAGAT
ENST00000393994.4:c.432+218_432+219insAGAT	ENSP00000377563.2:n.432+218_432+219insAGAT
ENST00000419755.3:c.543+218_543+219insAGAT	ENSP00000398526.3:n.543+218_543+219insAGAT
ENST00000455748.6:c.432+218_432+219insAGAT	ENSP00000405764.2:n.432+218_432+219insAGAT
ENST00000524458.5:c.*139+218_*139+219insAGAT	ENSP00000436195.1:n.*139+218_*139+219insAGAT
ENST00000524705.2:c.153+218_153+219insAGAT	ENSP00000436927.1:n.153+218_153+219insAGAT
ENST00000524907.5:n.422+218_422+219insAGAT
ENST00000525809.5:c.160-644_160-643insAGAT	ENSP00000431187.1:n.160-644_160-643insAGAT
ENST00000526035.5:c.*139+218_*139+219insAGAT	ENSP00000434197.1:n.*139+218_*139+219insAGAT
ENST00000526760.5:c.*139+218_*139+219insAGAT	ENSP00000432140.1:n.*139+218_*139+219insAGAT
ENST00000527251.5:c.*139+218_*139+219insAGAT	ENSP00000434360.1:n.*139+218_*139+219insAGAT
ENST00000529766.5:n.439+218_439+219insAGAT
ENST00000529953.5:n.84+218_84+219insAGAT
ENST00000529955.5:n.450+218_450+219insAGAT
ENST00000532908.5:c.*139+218_*139+219insAGAT	ENSP00000431866.1:n.*139+218_*139+219insAGAT
ENST00000533430.5:n.210+218_210+219insAGAT
ENST00000533557.5:c.*139+218_*139+219insAGAT	ENSP00000434619.1:n.*139+218_*139+219insAGAT
ENST00000533644.5:c.432+218_432+219insAGAT	ENSP00000436073.1:n.432+218_432+219insAGAT
ENST00000534730.5:n.444+218_444+219insAGAT
ENST00000630659.2:c.*139+218_*139+219insAGAT	ENSP00000486455.1:n.*139+218_*139+219insAGAT
NM_024649.4:c.432+218_432+219insAGAT	NP_078925.3:n.432+218_432+219insAGAT
NM_024649.5:c.432+218_432+219insAGAT MANE Select	NP_078925.3:n.432+218_432+219insAGAT