Canonical Allele Identifier: CA2574887147
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510768dup , CM000673.2:g.66510768dup GRCh38
NC_000011.9:g.66278239dup , CM000673.1:g.66278239dup GRCh37
NC_000011.8:g.66034815dup NCBI36
NG_009093.1:g.5121dup
NG_032068.1:g.35360dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.47+62dup MANE Select ENSP00000317469.7:n.47+62dup
ENST00000318312.11:c.47+62dup ENSP00000317469.7:n.47+62dup
ENST00000393994.4:c.47+62dup ENSP00000377563.2:n.47+62dup
ENST00000419755.3:c.159-245dup ENSP00000398526.3:n.159-245dup
ENST00000455748.6:c.47+62dup ENSP00000405764.2:n.47+62dup
ENST00000524907.5:n.37+62dup
ENST00000525809.5:c.47+62dup ENSP00000431187.1:n.47+62dup
ENST00000526035.5:c.47+62dup ENSP00000434197.1:n.47+62dup
ENST00000526760.5:c.47+62dup ENSP00000432140.1:n.47+62dup
ENST00000526815.5:c.-288dup ENSP00000436860.1:n.-288dup
ENST00000527251.5:c.-288dup ENSP00000434360.1:n.-288dup
ENST00000529766.5:n.54+62dup
ENST00000529955.5:n.65+62dup
ENST00000532908.5:c.47+62dup ENSP00000431866.1:n.47+62dup
ENST00000533557.5:c.47+62dup ENSP00000434619.1:n.47+62dup
ENST00000533644.5:c.47+62dup ENSP00000436073.1:n.47+62dup
ENST00000534730.5:n.59+62dup
ENST00000630659.2:c.47+62dup ENSP00000486455.1:n.47+62dup
NM_024649.4:c.47+62dup NP_078925.3:n.47+62dup
NM_024649.5:c.47+62dup MANE Select NP_078925.3:n.47+62dup