Canonical Allele Identifier: CA1979725949
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66519616G= , CM000673.2:g.66519616G= GRCh38
NC_000011.9:g.66287087G= , CM000673.1:g.66287087G= GRCh37
NC_000011.8:g.66043663G= NCBI36
NG_009093.1:g.13969G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.592-1G= MANE Select ENSP00000317469.7:n.592-1G=
ENST00000318312.11:c.592-1G= ENSP00000317469.7:n.592-1G=
ENST00000393994.4:c.592-1G= ENSP00000377563.2:n.592-1G=
ENST00000419755.3:c.703-1G= ENSP00000398526.3:n.703-1G=
ENST00000455748.6:c.433-1654G= ENSP00000405764.2:n.433-1654G=
ENST00000524458.5:c.*381-1G= ENSP00000436195.1:n.*381-1G=
ENST00000524907.5:n.688-1G=
ENST00000525809.5:c.319-1G= ENSP00000431187.1:n.319-1G=
ENST00000526035.5:c.*299-5G= ENSP00000434197.1:n.*299-5G=
ENST00000526760.5:c.*299-1G= ENSP00000432140.1:n.*299-1G=
ENST00000527251.5:c.*299-1G= ENSP00000434360.1:n.*299-1G=
ENST00000528543.1:n.114-1G=
ENST00000529766.5:n.599-1G=
ENST00000529953.5:n.244-1G=
ENST00000529955.5:n.563-1G=
ENST00000532908.5:c.*252-1G= ENSP00000431866.1:n.*252-1G=
ENST00000533430.5:n.370-1G=
ENST00000533557.5:c.*252-1G= ENSP00000434619.1:n.*252-1G=
ENST00000533644.5:c.*50-1G= ENSP00000436073.1:n.*50-1G=
ENST00000630659.2:c.*299-1G= ENSP00000486455.1:n.*299-1G=
NM_024649.4:c.592-1G= NP_078925.3:n.592-1G=
NM_024649.5:c.592-1G= MANE Select NP_078925.3:n.592-1G=