Canonical Allele Identifier: CA1979718706
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515705G= , CM000673.2:g.66515705G= GRCh38
NC_000011.9:g.66283176G= , CM000673.1:g.66283176G= GRCh37
NC_000011.8:g.66039752G= NCBI36
NG_009093.1:g.10058G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.492G= MANE Select ENSP00000317469.7:p.Glu164=
ENST00000318312.11:c.492G= ENSP00000317469.7:p.Glu164=
ENST00000393994.4:c.492G= ENSP00000377563.2:p.Glu164=
ENST00000419755.3:c.603G= ENSP00000398526.3:p.Glu201=
ENST00000455748.6:c.432+1027G= ENSP00000405764.2:n.432+1027G=
ENST00000524458.5:c.*152G= ENSP00000436195.1:n.*152G=
ENST00000524907.5:n.588G=
ENST00000525809.5:c.219G= ENSP00000431187.1:p.Glu73=
ENST00000526035.5:c.*199G= ENSP00000434197.1:n.*199G=
ENST00000526760.5:c.*199G= ENSP00000432140.1:n.*199G=
ENST00000527251.5:c.*199G= ENSP00000434360.1:n.*199G=
ENST00000528543.1:n.14G=
ENST00000529766.5:n.499G=
ENST00000529953.5:n.144G=
ENST00000529955.5:n.463G=
ENST00000532908.5:c.*152G= ENSP00000431866.1:n.*152G=
ENST00000533430.5:n.270G=
ENST00000533557.5:c.*152G= ENSP00000434619.1:n.*152G=
ENST00000533644.5:c.445G= ENSP00000436073.1:p.Gly149=
ENST00000534730.5:n.504G=
ENST00000630659.2:c.*199G= ENSP00000486455.1:n.*199G=
NM_024649.4:c.492G= NP_078925.3:p.Glu164=
NM_024649.5:c.492G= MANE Select NP_078925.3:p.Glu164=