Canonical Allele Identifier: CA1979718790
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515770A= , CM000673.2:g.66515770A= GRCh38
NC_000011.9:g.66283241A= , CM000673.1:g.66283241A= GRCh37
NC_000011.8:g.66039817A= NCBI36
NG_009093.1:g.10123A=

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.518+39A= MANE Select ENSP00000317469.7:n.518+39A=
ENST00000318312.11:c.518+39A= ENSP00000317469.7:n.518+39A=
ENST00000393994.4:c.518+39A= ENSP00000377563.2:n.518+39A=
ENST00000419755.3:c.629+39A= ENSP00000398526.3:n.629+39A=
ENST00000455748.6:c.432+1092A= ENSP00000405764.2:n.432+1092A=
ENST00000524458.5:c.*217A= ENSP00000436195.1:n.*217A=
ENST00000524907.5:n.614+39A=
ENST00000525809.5:c.245+39A= ENSP00000431187.1:n.245+39A=
ENST00000526035.5:c.*225+39A= ENSP00000434197.1:n.*225+39A=
ENST00000526760.5:c.*225+39A= ENSP00000432140.1:n.*225+39A=
ENST00000527251.5:c.*225+39A= ENSP00000434360.1:n.*225+39A=
ENST00000528543.1:n.40+39A=
ENST00000529766.5:n.525+39A=
ENST00000529953.5:n.170+39A=
ENST00000529955.5:n.489+39A=
ENST00000532908.5:c.*178+39A= ENSP00000431866.1:n.*178+39A=
ENST00000533430.5:n.296+39A=
ENST00000533557.5:c.*178+39A= ENSP00000434619.1:n.*178+39A=
ENST00000533644.5:c.471+39A= ENSP00000436073.1:n.471+39A=
ENST00000534730.5:n.569A=
ENST00000630659.2:c.*225+39A= ENSP00000486455.1:n.*225+39A=
NM_024649.4:c.518+39A= NP_078925.3:n.518+39A=
NM_024649.5:c.518+39A= MANE Select NP_078925.3:n.518+39A=