Canonical Allele Identifier: CA1979718427

Gene: BBS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515586G= , CM000673.2:g.66515586G=	GRCh38
NC_000011.9:g.66283057G= , CM000673.1:g.66283057G=	GRCh37
NC_000011.8:g.66039633G=	NCBI36
NG_009093.1:g.9939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.479G= MANE Select	ENSP00000317469.7:p.Arg160=
ENST00000318312.11:c.479G=	ENSP00000317469.7:p.Arg160=
ENST00000393994.4:c.479G=	ENSP00000377563.2:p.Arg160=
ENST00000419755.3:c.590G=	ENSP00000398526.3:p.Arg197=
ENST00000455748.6:c.432+908G=	ENSP00000405764.2:n.432+908G=
ENST00000524458.5:c.*140-107G=	ENSP00000436195.1:n.*140-107G=
ENST00000524705.2:c.200G=
ENST00000524907.5:n.469G=
ENST00000525809.5:c.206G=	ENSP00000431187.1:p.Arg69=
ENST00000526035.5:c.*186G=	ENSP00000434197.1:n.*186G=
ENST00000526760.5:c.*186G=	ENSP00000432140.1:n.*186G=
ENST00000527251.5:c.*186G=	ENSP00000434360.1:n.*186G=
ENST00000529766.5:n.486G=
ENST00000529953.5:n.131G=
ENST00000529955.5:n.451-107G=
ENST00000532908.5:c.*140-107G=	ENSP00000431866.1:n.*140-107G=
ENST00000533430.5:n.257G=
ENST00000533557.5:c.*140-107G=	ENSP00000434619.1:n.*140-107G=
ENST00000533644.5:c.433-107G=	ENSP00000436073.1:n.433-107G=
ENST00000534730.5:n.491G=
ENST00000630659.2:c.*186G=	ENSP00000486455.1:n.*186G=
NM_024649.4:c.479G=	NP_078925.3:p.Arg160=
NM_024649.5:c.479G= MANE Select	NP_078925.3:p.Arg160=