Canonical Allele Identifier: CA1979718286
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515515A= , CM000673.2:g.66515515A= GRCh38
NC_000011.9:g.66282986A= , CM000673.1:g.66282986A= GRCh37
NC_000011.8:g.66039562A= NCBI36
NG_009093.1:g.9868A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.433-25A= MANE Select ENSP00000317469.7:n.433-25A=
ENST00000318312.11:c.433-25A= ENSP00000317469.7:n.433-25A=
ENST00000393994.4:c.433-25A= ENSP00000377563.2:n.433-25A=
ENST00000419755.3:c.544-25A= ENSP00000398526.3:n.544-25A=
ENST00000455748.6:c.432+837A= ENSP00000405764.2:n.432+837A=
ENST00000524458.5:c.*140-178A= ENSP00000436195.1:n.*140-178A=
ENST00000524705.2:c.154-25A= ENSP00000436927.1:n.154-25A=
ENST00000524907.5:n.423-25A=
ENST00000525809.5:c.160-25A= ENSP00000431187.1:n.160-25A=
ENST00000526035.5:c.*140-25A= ENSP00000434197.1:n.*140-25A=
ENST00000526760.5:c.*140-25A= ENSP00000432140.1:n.*140-25A=
ENST00000527251.5:c.*140-25A= ENSP00000434360.1:n.*140-25A=
ENST00000529766.5:n.440-25A=
ENST00000529953.5:n.85-25A=
ENST00000529955.5:n.451-178A=
ENST00000532908.5:c.*140-178A= ENSP00000431866.1:n.*140-178A=
ENST00000533430.5:n.211-25A=
ENST00000533557.5:c.*140-178A= ENSP00000434619.1:n.*140-178A=
ENST00000533644.5:c.433-178A= ENSP00000436073.1:n.433-178A=
ENST00000534730.5:n.445-25A=
ENST00000630659.2:c.*140-25A= ENSP00000486455.1:n.*140-25A=
NM_024649.4:c.433-25A= NP_078925.3:n.433-25A=
NM_024649.5:c.433-25A= MANE Select NP_078925.3:n.433-25A=