Canonical Allele Identifier: CA2839783137
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514593del , CM000673.2:g.66514593del GRCh38
NC_000011.9:g.66282064del , CM000673.1:g.66282064del GRCh37
NC_000011.8:g.66038640del NCBI36
NG_009093.1:g.8946del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.347del MANE Select ENSP00000317469.7:p.Lys116ArgfsTer?
ENST00000318312.11:c.347del ENSP00000317469.7:p.Lys116ArgfsTer?
ENST00000393994.4:c.347del ENSP00000377563.2:p.Lys116ArgfsTer?
ENST00000419755.3:c.458del ENSP00000398526.3:p.Lys153ArgfsTer?
ENST00000455748.6:c.347del ENSP00000405764.2:p.Lys116ArgfsTer30
ENST00000524458.5:c.*54del ENSP00000436195.1:n.*54del
ENST00000524705.2:c.68del ENSP00000436927.1:p.Lys23ArgfsTer?
ENST00000524907.5:n.337del
ENST00000525809.5:c.160-947del ENSP00000431187.1:n.160-947del
ENST00000526035.5:c.*54del ENSP00000434197.1:n.*54del
ENST00000526760.5:c.*54del ENSP00000432140.1:n.*54del
ENST00000527251.5:c.*54del ENSP00000434360.1:n.*54del
ENST00000529766.5:n.354del
ENST00000529955.5:n.365del
ENST00000532908.5:c.*54del ENSP00000431866.1:n.*54del
ENST00000533430.5:n.125del
ENST00000533557.5:c.*54del ENSP00000434619.1:n.*54del
ENST00000533644.5:c.347del ENSP00000436073.1:p.Lys116ArgfsTer?
ENST00000534730.5:n.359del
ENST00000630659.2:c.*54del ENSP00000486455.1:n.*54del
NM_024649.4:c.347del NP_078925.3:p.Lys116ArgfsTer?
NM_024649.5:c.347del MANE Select NP_078925.3:p.Lys116ArgfsTer?