Canonical Allele Identifier: CA381457409

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66283168A>G (hg19) ; chr11:g.66515697A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515697A>G , CM000673.2:g.66515697A>G	GRCh38
NC_000011.9:g.66283168A>G , CM000673.1:g.66283168A>G	GRCh37
NC_000011.8:g.66039744A>G	NCBI36
NG_009093.1:g.10050A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.484A>G MANE Select	ENSP00000317469.7:p.Thr162Ala
ENST00000318312.11:c.484A>G	ENSP00000317469.7:p.Thr162Ala
ENST00000393994.4:c.484A>G	ENSP00000377563.2:p.Thr162Ala
ENST00000419755.3:c.595A>G	ENSP00000398526.3:p.Thr199Ala
ENST00000455748.6:c.432+1019A>G	ENSP00000405764.2:n.432+1019A>G
ENST00000524458.5:c.*144A>G	ENSP00000436195.1:n.*144A>G
ENST00000524907.5:n.580A>G
ENST00000525809.5:c.211A>G	ENSP00000431187.1:p.Thr71Ala
ENST00000526035.5:c.*191A>G	ENSP00000434197.1:n.*191A>G
ENST00000526760.5:c.*191A>G	ENSP00000432140.1:n.*191A>G
ENST00000527251.5:c.*191A>G	ENSP00000434360.1:n.*191A>G
ENST00000528543.1:n.6A>G
ENST00000529766.5:n.491A>G
ENST00000529953.5:n.136A>G
ENST00000529955.5:n.455A>G
ENST00000532908.5:c.*144A>G	ENSP00000431866.1:n.*144A>G
ENST00000533430.5:n.262A>G
ENST00000533557.5:c.*144A>G	ENSP00000434619.1:n.*144A>G
ENST00000533644.5:c.437A>G	ENSP00000436073.1:p.Asp146Gly
ENST00000534730.5:n.496A>G
ENST00000630659.2:c.*191A>G	ENSP00000486455.1:n.*191A>G
NM_024649.4:c.484A>G	NP_078925.3:p.Thr162Ala
NM_024649.5:c.484A>G MANE Select	NP_078925.3:p.Thr162Ala