Canonical Allele Identifier: CA1979718693

Gene: BBS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515699G= , CM000673.2:g.66515699G=	GRCh38
NC_000011.9:g.66283170G= , CM000673.1:g.66283170G=	GRCh37
NC_000011.8:g.66039746G=	NCBI36
NG_009093.1:g.10052G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.486G= MANE Select	ENSP00000317469.7:p.Thr162=
ENST00000318312.11:c.486G=	ENSP00000317469.7:p.Thr162=
ENST00000393994.4:c.486G=	ENSP00000377563.2:p.Thr162=
ENST00000419755.3:c.597G=	ENSP00000398526.3:p.Thr199=
ENST00000455748.6:c.432+1021G=	ENSP00000405764.2:n.432+1021G=
ENST00000524458.5:c.*146G=	ENSP00000436195.1:n.*146G=
ENST00000524907.5:n.582G=
ENST00000525809.5:c.213G=	ENSP00000431187.1:p.Thr71=
ENST00000526035.5:c.*193G=	ENSP00000434197.1:n.*193G=
ENST00000526760.5:c.*193G=	ENSP00000432140.1:n.*193G=
ENST00000527251.5:c.*193G=	ENSP00000434360.1:n.*193G=
ENST00000528543.1:n.8G=
ENST00000529766.5:n.493G=
ENST00000529953.5:n.138G=
ENST00000529955.5:n.457G=
ENST00000532908.5:c.*146G=	ENSP00000431866.1:n.*146G=
ENST00000533430.5:n.264G=
ENST00000533557.5:c.*146G=	ENSP00000434619.1:n.*146G=
ENST00000533644.5:c.439G=	ENSP00000436073.1:p.Gly147=
ENST00000534730.5:n.498G=
ENST00000630659.2:c.*193G=	ENSP00000486455.1:n.*193G=
NM_024649.4:c.486G=	NP_078925.3:p.Thr162=
NM_024649.5:c.486G= MANE Select	NP_078925.3:p.Thr162=