Canonical Allele Identifier: CA1979716316
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514386G= , CM000673.2:g.66514386G= GRCh38
NC_000011.9:g.66281857G= , CM000673.1:g.66281857G= GRCh37
NC_000011.8:g.66038433G= NCBI36
NG_009093.1:g.8739G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.160-20G= MANE Select ENSP00000317469.7:n.160-20G=
ENST00000318312.11:c.160-20G= ENSP00000317469.7:n.160-20G=
ENST00000393994.4:c.160-20G= ENSP00000377563.2:n.160-20G=
ENST00000419755.3:c.271-20G= ENSP00000398526.3:n.271-20G=
ENST00000455748.6:c.160-20G= ENSP00000405764.2:n.160-20G=
ENST00000524458.5:c.35-20G= ENSP00000436195.1:n.35-20G=
ENST00000524705.2:c.-20-120G= ENSP00000436927.1:n.-20-120G=
ENST00000524907.5:n.150-20G=
ENST00000525809.5:c.160-1154G= ENSP00000431187.1:n.160-1154G=
ENST00000526035.5:c.125-20G= ENSP00000434197.1:n.125-20G=
ENST00000526760.5:c.125-20G= ENSP00000432140.1:n.125-20G=
ENST00000526815.5:c.70-20G= ENSP00000436860.1:n.70-20G=
ENST00000527251.5:c.35-20G= ENSP00000434360.1:n.35-20G=
ENST00000529766.5:n.167-20G=
ENST00000529955.5:n.178-20G=
ENST00000532908.5:c.125-20G= ENSP00000431866.1:n.125-20G=
ENST00000533557.5:c.125-20G= ENSP00000434619.1:n.125-20G=
ENST00000533644.5:c.160-20G= ENSP00000436073.1:n.160-20G=
ENST00000534730.5:n.172-20G=
ENST00000630659.2:c.125-20G= ENSP00000486455.1:n.125-20G=
NM_024649.4:c.160-20G= NP_078925.3:n.160-20G=
NM_024649.5:c.160-20G= MANE Select NP_078925.3:n.160-20G=