Canonical Allele Identifier: CA224073849

Gene: BBS1

Linked Data

• dbSNP Id: rs35306986
• MyVariant Identifiers: chr11:g.66283358_66283359insG (hg19) ; chr11:g.66515887_66515888insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515889dup , CM000673.2:g.66515889dup	GRCh38
NC_000011.9:g.66283360dup , CM000673.1:g.66283360dup	GRCh37
NC_000011.8:g.66039936dup	NCBI36
NG_009093.1:g.10242dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.547dup MANE Select	ENSP00000317469.7:p.Glu183GlyfsTer30
ENST00000318312.11:c.547dup	ENSP00000317469.7:p.Glu183GlyfsTer30
ENST00000393994.4:c.547dup	ENSP00000377563.2:p.Glu183GlyfsTer30
ENST00000419755.3:c.658dup	ENSP00000398526.3:p.Glu220GlyfsTer30
ENST00000455748.6:c.432+1211dup	ENSP00000405764.2:n.432+1211dup
ENST00000524458.5:c.*336dup	ENSP00000436195.1:n.*336dup
ENST00000524907.5:n.643dup
ENST00000525809.5:c.274dup	ENSP00000431187.1:p.Glu92GlyfsTer30
ENST00000526035.5:c.*254dup	ENSP00000434197.1:n.*254dup
ENST00000526760.5:c.*254dup	ENSP00000432140.1:n.*254dup
ENST00000527251.5:c.*254dup	ENSP00000434360.1:n.*254dup
ENST00000528543.1:n.69dup
ENST00000529766.5:n.554dup
ENST00000529953.5:n.199dup
ENST00000529955.5:n.518dup
ENST00000532908.5:c.*207dup	ENSP00000431866.1:n.*207dup
ENST00000533430.5:n.325dup
ENST00000533557.5:c.*207dup	ENSP00000434619.1:n.*207dup
ENST00000533644.5:c.*5dup	ENSP00000436073.1:n.*5dup
ENST00000630659.2:c.*254dup	ENSP00000486455.1:n.*254dup
NM_024649.4:c.547dup	NP_078925.3:p.Glu183GlyfsTer30
NM_024649.5:c.547dup MANE Select	NP_078925.3:p.Glu183GlyfsTer30