Canonical Allele Identifier: CA2840488861
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514462del , CM000673.2:g.66514462del GRCh38
NC_000011.9:g.66281933del , CM000673.1:g.66281933del GRCh37
NC_000011.8:g.66038509del NCBI36
NG_009093.1:g.8815del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.216del MANE Select ENSP00000317469.7:p.Gly73AspfsTer4
ENST00000318312.11:c.216del ENSP00000317469.7:p.Gly73AspfsTer4
ENST00000393994.4:c.216del ENSP00000377563.2:p.Gly73AspfsTer4
ENST00000419755.3:c.327del ENSP00000398526.3:p.Gly110AspfsTer4
ENST00000455748.6:c.216del ENSP00000405764.2:p.Gly73AspfsTer4
ENST00000524458.5:c.91del ENSP00000436195.1:p.Arg31GlyfsTer?
ENST00000524705.2:c.-20-44del ENSP00000436927.1:n.-20-44del
ENST00000524907.5:n.206del
ENST00000525809.5:c.160-1078del ENSP00000431187.1:n.160-1078del
ENST00000526035.5:c.181del ENSP00000434197.1:p.Arg61GlyfsTer?
ENST00000526760.5:c.181del ENSP00000432140.1:p.Arg61GlyfsTer?
ENST00000526815.5:c.126del ENSP00000436860.1:p.Gly43AspfsTer4
ENST00000527251.5:c.91del ENSP00000434360.1:p.Arg31GlyfsTer?
ENST00000529766.5:n.223del
ENST00000529955.5:n.234del
ENST00000532908.5:c.181del ENSP00000431866.1:p.Arg61GlyfsTer?
ENST00000533557.5:c.181del ENSP00000434619.1:p.Arg61GlyfsTer?
ENST00000533644.5:c.216del ENSP00000436073.1:p.Gly73AspfsTer4
ENST00000534730.5:n.228del
ENST00000630659.2:c.181del ENSP00000486455.1:p.Arg61GlyfsTer?
NM_024649.4:c.216del NP_078925.3:p.Gly73AspfsTer4
NM_024649.5:c.216del MANE Select NP_078925.3:p.Gly73AspfsTer4