Canonical Allele Identifier: CA1979716546

Gene: BBS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514461A= , CM000673.2:g.66514461A=	GRCh38
NC_000011.9:g.66281932A= , CM000673.1:g.66281932A=	GRCh37
NC_000011.8:g.66038508A=	NCBI36
NG_009093.1:g.8814A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.215A= MANE Select	ENSP00000317469.7:p.Lys72=
ENST00000318312.11:c.215A=	ENSP00000317469.7:p.Lys72=
ENST00000393994.4:c.215A=	ENSP00000377563.2:p.Lys72=
ENST00000419755.3:c.326A=	ENSP00000398526.3:p.Lys109=
ENST00000455748.6:c.215A=	ENSP00000405764.2:p.Lys72=
ENST00000524458.5:c.90A=	ENSP00000436195.1:p.Gln30=
ENST00000524705.2:c.-20-45A=	ENSP00000436927.1:n.-20-45A=
ENST00000524907.5:n.205A=
ENST00000525809.5:c.160-1079A=	ENSP00000431187.1:n.160-1079A=
ENST00000526035.5:c.180A=	ENSP00000434197.1:p.Gln60=
ENST00000526760.5:c.180A=	ENSP00000432140.1:p.Gln60=
ENST00000526815.5:c.125A=	ENSP00000436860.1:p.Lys42=
ENST00000527251.5:c.90A=	ENSP00000434360.1:p.Gln30=
ENST00000529766.5:n.222A=
ENST00000529955.5:n.233A=
ENST00000532908.5:c.180A=	ENSP00000431866.1:p.Gln60=
ENST00000533557.5:c.180A=	ENSP00000434619.1:p.Gln60=
ENST00000533644.5:c.215A=	ENSP00000436073.1:p.Lys72=
ENST00000534730.5:n.227A=
ENST00000630659.2:c.180A=	ENSP00000486455.1:p.Gln60=
NM_024649.4:c.215A=	NP_078925.3:p.Lys72=
NM_024649.5:c.215A= MANE Select	NP_078925.3:p.Lys72=