Canonical Allele Identifier: CA1979716997
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514662G= , CM000673.2:g.66514662G= GRCh38
NC_000011.9:g.66282133G= , CM000673.1:g.66282133G= GRCh37
NC_000011.8:g.66038709G= NCBI36
NG_009093.1:g.9015G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.416G= MANE Select ENSP00000317469.7:p.Trp139=
ENST00000318312.11:c.416G= ENSP00000317469.7:p.Trp139=
ENST00000393994.4:c.416G= ENSP00000377563.2:p.Trp139=
ENST00000419755.3:c.527G= ENSP00000398526.3:p.Trp176=
ENST00000455748.6:c.416G= ENSP00000405764.2:p.Trp139=
ENST00000524458.5:c.*123G= ENSP00000436195.1:n.*123G=
ENST00000524705.2:c.137G= ENSP00000436927.1:p.Trp46=
ENST00000524907.5:n.406G=
ENST00000525809.5:c.160-878G= ENSP00000431187.1:n.160-878G=
ENST00000526035.5:c.*123G= ENSP00000434197.1:n.*123G=
ENST00000526760.5:c.*123G= ENSP00000432140.1:n.*123G=
ENST00000527251.5:c.*123G= ENSP00000434360.1:n.*123G=
ENST00000529766.5:n.423G=
ENST00000529953.5:n.68G=
ENST00000529955.5:n.434G=
ENST00000532908.5:c.*123G= ENSP00000431866.1:n.*123G=
ENST00000533430.5:n.194G=
ENST00000533557.5:c.*123G= ENSP00000434619.1:n.*123G=
ENST00000533644.5:c.416G= ENSP00000436073.1:p.Trp139=
ENST00000534730.5:n.428G=
ENST00000630659.2:c.*123G= ENSP00000486455.1:n.*123G=
NM_024649.4:c.416G= NP_078925.3:p.Trp139=
NM_024649.5:c.416G= MANE Select NP_078925.3:p.Trp139=