Canonical Allele Identifier: CA1979718284
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515513A= , CM000673.2:g.66515513A= GRCh38
NC_000011.9:g.66282984A= , CM000673.1:g.66282984A= GRCh37
NC_000011.8:g.66039560A= NCBI36
NG_009093.1:g.9866A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.433-27A= MANE Select ENSP00000317469.7:n.433-27A=
ENST00000318312.11:c.433-27A= ENSP00000317469.7:n.433-27A=
ENST00000393994.4:c.433-27A= ENSP00000377563.2:n.433-27A=
ENST00000419755.3:c.544-27A= ENSP00000398526.3:n.544-27A=
ENST00000455748.6:c.432+835A= ENSP00000405764.2:n.432+835A=
ENST00000524458.5:c.*140-180A= ENSP00000436195.1:n.*140-180A=
ENST00000524705.2:c.154-27A= ENSP00000436927.1:n.154-27A=
ENST00000524907.5:n.423-27A=
ENST00000525809.5:c.160-27A= ENSP00000431187.1:n.160-27A=
ENST00000526035.5:c.*140-27A= ENSP00000434197.1:n.*140-27A=
ENST00000526760.5:c.*140-27A= ENSP00000432140.1:n.*140-27A=
ENST00000527251.5:c.*140-27A= ENSP00000434360.1:n.*140-27A=
ENST00000529766.5:n.440-27A=
ENST00000529953.5:n.85-27A=
ENST00000529955.5:n.451-180A=
ENST00000532908.5:c.*140-180A= ENSP00000431866.1:n.*140-180A=
ENST00000533430.5:n.211-27A=
ENST00000533557.5:c.*140-180A= ENSP00000434619.1:n.*140-180A=
ENST00000533644.5:c.433-180A= ENSP00000436073.1:n.433-180A=
ENST00000534730.5:n.445-27A=
ENST00000630659.2:c.*140-27A= ENSP00000486455.1:n.*140-27A=
NM_024649.4:c.433-27A= NP_078925.3:n.433-27A=
NM_024649.5:c.433-27A= MANE Select NP_078925.3:n.433-27A=