Canonical Allele Identifier: CA599875355
Gene: BBS1 HGNC NCBI

Linked Data

dbSNP Id: rs1307831178

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514834_66514841del , CM000673.2:g.66514834_66514841del GRCh38
NC_000011.9:g.66282305_66282312del , CM000673.1:g.66282305_66282312del GRCh37
NC_000011.8:g.66038881_66038888del NCBI36
NG_009093.1:g.9187_9194del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.432+156_432+163del MANE Select ENSP00000317469.7:n.432+156_432+163del
ENST00000318312.11:c.432+156_432+163del ENSP00000317469.7:n.432+156_432+163del
ENST00000393994.4:c.432+156_432+163del ENSP00000377563.2:n.432+156_432+163del
ENST00000419755.3:c.543+156_543+163del ENSP00000398526.3:n.543+156_543+163del
ENST00000455748.6:c.432+156_432+163del ENSP00000405764.2:n.432+156_432+163del
ENST00000524458.5:c.*139+156_*139+163del ENSP00000436195.1:n.*139+156_*139+163del
ENST00000524705.2:c.153+156_153+163del ENSP00000436927.1:n.153+156_153+163del
ENST00000524907.5:n.422+156_422+163del
ENST00000525809.5:c.160-706_160-699del ENSP00000431187.1:n.160-706_160-699del
ENST00000526035.5:c.*139+156_*139+163del ENSP00000434197.1:n.*139+156_*139+163del
ENST00000526760.5:c.*139+156_*139+163del ENSP00000432140.1:n.*139+156_*139+163del
ENST00000527251.5:c.*139+156_*139+163del ENSP00000434360.1:n.*139+156_*139+163del
ENST00000529766.5:n.439+156_439+163del
ENST00000529953.5:n.84+156_84+163del
ENST00000529955.5:n.450+156_450+163del
ENST00000532908.5:c.*139+156_*139+163del ENSP00000431866.1:n.*139+156_*139+163del
ENST00000533430.5:n.210+156_210+163del
ENST00000533557.5:c.*139+156_*139+163del ENSP00000434619.1:n.*139+156_*139+163del
ENST00000533644.5:c.432+156_432+163del ENSP00000436073.1:n.432+156_432+163del
ENST00000534730.5:n.444+156_444+163del
ENST00000630659.2:c.*139+156_*139+163del ENSP00000486455.1:n.*139+156_*139+163del
NM_024649.4:c.432+156_432+163del NP_078925.3:n.432+156_432+163del
NM_024649.5:c.432+156_432+163del MANE Select NP_078925.3:n.432+156_432+163del