Canonical Allele Identifier: CA1979718280
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515511T= , CM000673.2:g.66515511T= GRCh38
NC_000011.9:g.66282982T= , CM000673.1:g.66282982T= GRCh37
NC_000011.8:g.66039558T= NCBI36
NG_009093.1:g.9864T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.433-29T= MANE Select ENSP00000317469.7:n.433-29T=
ENST00000318312.11:c.433-29T= ENSP00000317469.7:n.433-29T=
ENST00000393994.4:c.433-29T= ENSP00000377563.2:n.433-29T=
ENST00000419755.3:c.544-29T= ENSP00000398526.3:n.544-29T=
ENST00000455748.6:c.432+833T= ENSP00000405764.2:n.432+833T=
ENST00000524458.5:c.*140-182T= ENSP00000436195.1:n.*140-182T=
ENST00000524705.2:c.154-29T= ENSP00000436927.1:n.154-29T=
ENST00000524907.5:n.423-29T=
ENST00000525809.5:c.160-29T= ENSP00000431187.1:n.160-29T=
ENST00000526035.5:c.*140-29T= ENSP00000434197.1:n.*140-29T=
ENST00000526760.5:c.*140-29T= ENSP00000432140.1:n.*140-29T=
ENST00000527251.5:c.*140-29T= ENSP00000434360.1:n.*140-29T=
ENST00000529766.5:n.440-29T=
ENST00000529953.5:n.85-29T=
ENST00000529955.5:n.451-182T=
ENST00000532908.5:c.*140-182T= ENSP00000431866.1:n.*140-182T=
ENST00000533430.5:n.211-29T=
ENST00000533557.5:c.*140-182T= ENSP00000434619.1:n.*140-182T=
ENST00000533644.5:c.433-182T= ENSP00000436073.1:n.433-182T=
ENST00000534730.5:n.445-29T=
ENST00000630659.2:c.*140-29T= ENSP00000486455.1:n.*140-29T=
NM_024649.4:c.433-29T= NP_078925.3:n.433-29T=
NM_024649.5:c.433-29T= MANE Select NP_078925.3:n.433-29T=