Canonical Allele Identifier: CA381457569

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66283366T>C (hg19) ; chr11:g.66515895T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515895T>C , CM000673.2:g.66515895T>C	GRCh38
NC_000011.9:g.66283366T>C , CM000673.1:g.66283366T>C	GRCh37
NC_000011.8:g.66039942T>C	NCBI36
NG_009093.1:g.10248T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.553T>C MANE Select	ENSP00000317469.7:p.Phe185Leu
ENST00000318312.11:c.553T>C	ENSP00000317469.7:p.Phe185Leu
ENST00000393994.4:c.553T>C	ENSP00000377563.2:p.Phe185Leu
ENST00000419755.3:c.664T>C	ENSP00000398526.3:p.Phe222Leu
ENST00000455748.6:c.432+1217T>C	ENSP00000405764.2:n.432+1217T>C
ENST00000524458.5:c.*342T>C	ENSP00000436195.1:n.*342T>C
ENST00000524907.5:n.649T>C
ENST00000525809.5:c.280T>C	ENSP00000431187.1:p.Phe94Leu
ENST00000526035.5:c.*260T>C	ENSP00000434197.1:n.*260T>C
ENST00000526760.5:c.*260T>C	ENSP00000432140.1:n.*260T>C
ENST00000527251.5:c.*260T>C	ENSP00000434360.1:n.*260T>C
ENST00000528543.1:n.75T>C
ENST00000529766.5:n.560T>C
ENST00000529953.5:n.205T>C
ENST00000529955.5:n.524T>C
ENST00000532908.5:c.*213T>C	ENSP00000431866.1:n.*213T>C
ENST00000533430.5:n.331T>C
ENST00000533557.5:c.*213T>C	ENSP00000434619.1:n.*213T>C
ENST00000533644.5:c.*11T>C	ENSP00000436073.1:n.*11T>C
ENST00000630659.2:c.*260T>C	ENSP00000486455.1:n.*260T>C
NM_024649.4:c.553T>C	NP_078925.3:p.Phe185Leu
NM_024649.5:c.553T>C MANE Select	NP_078925.3:p.Phe185Leu