Canonical Allele Identifier: CA1979716666

Gene: BBS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514494C= , CM000673.2:g.66514494C=	GRCh38
NC_000011.9:g.66281965C= , CM000673.1:g.66281965C=	GRCh37
NC_000011.8:g.66038541C=	NCBI36
NG_009093.1:g.8847C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.248C= MANE Select	ENSP00000317469.7:p.Pro83=
ENST00000318312.11:c.248C=	ENSP00000317469.7:p.Pro83=
ENST00000393994.4:c.248C=	ENSP00000377563.2:p.Pro83=
ENST00000419755.3:c.359C=	ENSP00000398526.3:p.Pro120=
ENST00000455748.6:c.248C=	ENSP00000405764.2:p.Pro83=
ENST00000524458.5:c.123C=	ENSP00000436195.1:p.Thr41=
ENST00000524705.2:c.-20-12C=	ENSP00000436927.1:n.-20-12C=
ENST00000524907.5:n.238C=
ENST00000525809.5:c.160-1046C=	ENSP00000431187.1:n.160-1046C=
ENST00000526035.5:c.213C=	ENSP00000434197.1:p.Thr71=
ENST00000526760.5:c.213C=	ENSP00000432140.1:p.Thr71=
ENST00000526815.5:c.158C=	ENSP00000436860.1:p.Pro53=
ENST00000527251.5:c.123C=	ENSP00000434360.1:p.Thr41=
ENST00000529766.5:n.255C=
ENST00000529955.5:n.266C=
ENST00000532908.5:c.213C=	ENSP00000431866.1:p.Thr71=
ENST00000533430.5:n.26C=
ENST00000533557.5:c.213C=	ENSP00000434619.1:p.Thr71=
ENST00000533644.5:c.248C=	ENSP00000436073.1:p.Pro83=
ENST00000534730.5:n.260C=
ENST00000630659.2:c.213C=	ENSP00000486455.1:p.Thr71=
NM_024649.4:c.248C=	NP_078925.3:p.Pro83=
NM_024649.5:c.248C= MANE Select	NP_078925.3:p.Pro83=