Canonical Allele Identifier: CA1139662033

Gene: BBS1

Linked Data

• ClinVar Variation Id: 961524
• ClinVar RCV Id: RCV001235230
• dbSNP Id: rs1856010064

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514565dup , CM000673.2:g.66514565dup	GRCh38
NC_000011.9:g.66282036dup , CM000673.1:g.66282036dup	GRCh37
NC_000011.8:g.66038612dup	NCBI36
NG_009093.1:g.8918dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.319dup MANE Select	ENSP00000317469.7:p.Ala107GlyfsTer10
ENST00000318312.11:c.319dup	ENSP00000317469.7:p.Ala107GlyfsTer10
ENST00000393994.4:c.319dup	ENSP00000377563.2:p.Ala107GlyfsTer10
ENST00000419755.3:c.430dup	ENSP00000398526.3:p.Ala144GlyfsTer10
ENST00000455748.6:c.319dup	ENSP00000405764.2:p.Ala107GlyfsTer10
ENST00000524458.5:c.*26dup	ENSP00000436195.1:n.*26dup
ENST00000524705.2:c.40dup	ENSP00000436927.1:p.Ala14GlyfsTer10
ENST00000524907.5:n.309dup
ENST00000525809.5:c.160-975dup	ENSP00000431187.1:n.160-975dup
ENST00000526035.5:c.*26dup	ENSP00000434197.1:n.*26dup
ENST00000526760.5:c.*26dup	ENSP00000432140.1:n.*26dup
ENST00000527251.5:c.*26dup	ENSP00000434360.1:n.*26dup
ENST00000529766.5:n.326dup
ENST00000529955.5:n.337dup
ENST00000532908.5:c.*26dup	ENSP00000431866.1:n.*26dup
ENST00000533430.5:n.97dup
ENST00000533557.5:c.*26dup	ENSP00000434619.1:n.*26dup
ENST00000533644.5:c.319dup	ENSP00000436073.1:p.Ala107GlyfsTer10
ENST00000534730.5:n.331dup
ENST00000630659.2:c.*26dup	ENSP00000486455.1:n.*26dup
NM_024649.4:c.319dup	NP_078925.3:p.Ala107GlyfsTer10
NM_024649.5:c.319dup MANE Select	NP_078925.3:p.Ala107GlyfsTer10