Canonical Allele Identifier: CA2792478548
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514811_66514812insACA , CM000673.2:g.66514811_66514812insACA GRCh38
NC_000011.9:g.66282282_66282283insACA , CM000673.1:g.66282282_66282283insACA GRCh37
NC_000011.8:g.66038858_66038859insACA NCBI36
NG_009093.1:g.9164_9165insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.432+133_432+134insACA MANE Select ENSP00000317469.7:n.432+133_432+134insACA
ENST00000318312.11:c.432+133_432+134insACA ENSP00000317469.7:n.432+133_432+134insACA
ENST00000393994.4:c.432+133_432+134insACA ENSP00000377563.2:n.432+133_432+134insACA
ENST00000419755.3:c.543+133_543+134insACA ENSP00000398526.3:n.543+133_543+134insACA
ENST00000455748.6:c.432+133_432+134insACA ENSP00000405764.2:n.432+133_432+134insACA
ENST00000524458.5:c.*139+133_*139+134insACA ENSP00000436195.1:n.*139+133_*139+134insACA
ENST00000524705.2:c.153+133_153+134insACA ENSP00000436927.1:n.153+133_153+134insACA
ENST00000524907.5:n.422+133_422+134insACA
ENST00000525809.5:c.160-729_160-728insACA ENSP00000431187.1:n.160-729_160-728insACA
ENST00000526035.5:c.*139+133_*139+134insACA ENSP00000434197.1:n.*139+133_*139+134insACA
ENST00000526760.5:c.*139+133_*139+134insACA ENSP00000432140.1:n.*139+133_*139+134insACA
ENST00000527251.5:c.*139+133_*139+134insACA ENSP00000434360.1:n.*139+133_*139+134insACA
ENST00000529766.5:n.439+133_439+134insACA
ENST00000529953.5:n.84+133_84+134insACA
ENST00000529955.5:n.450+133_450+134insACA
ENST00000532908.5:c.*139+133_*139+134insACA ENSP00000431866.1:n.*139+133_*139+134insACA
ENST00000533430.5:n.210+133_210+134insACA
ENST00000533557.5:c.*139+133_*139+134insACA ENSP00000434619.1:n.*139+133_*139+134insACA
ENST00000533644.5:c.432+133_432+134insACA ENSP00000436073.1:n.432+133_432+134insACA
ENST00000534730.5:n.444+133_444+134insACA
ENST00000630659.2:c.*139+133_*139+134insACA ENSP00000486455.1:n.*139+133_*139+134insACA
NM_024649.4:c.432+133_432+134insACA NP_078925.3:n.432+133_432+134insACA
NM_024649.5:c.432+133_432+134insACA MANE Select NP_078925.3:n.432+133_432+134insACA