Canonical Allele Identifier: CA1979716335
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514392T= , CM000673.2:g.66514392T= GRCh38
NC_000011.9:g.66281863T= , CM000673.1:g.66281863T= GRCh37
NC_000011.8:g.66038439T= NCBI36
NG_009093.1:g.8745T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.160-14T= MANE Select ENSP00000317469.7:n.160-14T=
ENST00000318312.11:c.160-14T= ENSP00000317469.7:n.160-14T=
ENST00000393994.4:c.160-14T= ENSP00000377563.2:n.160-14T=
ENST00000419755.3:c.271-14T= ENSP00000398526.3:n.271-14T=
ENST00000455748.6:c.160-14T= ENSP00000405764.2:n.160-14T=
ENST00000524458.5:c.35-14T= ENSP00000436195.1:n.35-14T=
ENST00000524705.2:c.-20-114T= ENSP00000436927.1:n.-20-114T=
ENST00000524907.5:n.150-14T=
ENST00000525809.5:c.160-1148T= ENSP00000431187.1:n.160-1148T=
ENST00000526035.5:c.125-14T= ENSP00000434197.1:n.125-14T=
ENST00000526760.5:c.125-14T= ENSP00000432140.1:n.125-14T=
ENST00000526815.5:c.70-14T= ENSP00000436860.1:n.70-14T=
ENST00000527251.5:c.35-14T= ENSP00000434360.1:n.35-14T=
ENST00000529766.5:n.167-14T=
ENST00000529955.5:n.178-14T=
ENST00000532908.5:c.125-14T= ENSP00000431866.1:n.125-14T=
ENST00000533557.5:c.125-14T= ENSP00000434619.1:n.125-14T=
ENST00000533644.5:c.160-14T= ENSP00000436073.1:n.160-14T=
ENST00000534730.5:n.172-14T=
ENST00000630659.2:c.125-14T= ENSP00000486455.1:n.125-14T=
NM_024649.4:c.160-14T= NP_078925.3:n.160-14T=
NM_024649.5:c.160-14T= MANE Select NP_078925.3:n.160-14T=