Canonical Allele Identifier: CA1979716687

Gene: BBS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514513T= , CM000673.2:g.66514513T=	GRCh38
NC_000011.9:g.66281984T= , CM000673.1:g.66281984T=	GRCh37
NC_000011.8:g.66038560T=	NCBI36
NG_009093.1:g.8866T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.267T= MANE Select	ENSP00000317469.7:p.Ala89=
ENST00000318312.11:c.267T=	ENSP00000317469.7:p.Ala89=
ENST00000393994.4:c.267T=	ENSP00000377563.2:p.Ala89=
ENST00000419755.3:c.378T=	ENSP00000398526.3:p.Ala126=
ENST00000455748.6:c.267T=	ENSP00000405764.2:p.Ala89=
ENST00000524458.5:c.142T=	ENSP00000436195.1:p.Cys48=
ENST00000524705.2:c.-13T=	ENSP00000436927.1:n.-13T=
ENST00000524907.5:n.257T=
ENST00000525809.5:c.160-1027T=	ENSP00000431187.1:n.160-1027T=
ENST00000526035.5:c.232T=	ENSP00000434197.1:p.Cys78=
ENST00000526760.5:c.232T=	ENSP00000432140.1:p.Cys78=
ENST00000527251.5:c.142T=	ENSP00000434360.1:p.Cys48=
ENST00000529766.5:n.274T=
ENST00000529955.5:n.285T=
ENST00000532908.5:c.232T=	ENSP00000431866.1:p.Cys78=
ENST00000533430.5:n.45T=
ENST00000533557.5:c.232T=	ENSP00000434619.1:p.Cys78=
ENST00000533644.5:c.267T=	ENSP00000436073.1:p.Ala89=
ENST00000534730.5:n.279T=
ENST00000630659.2:c.232T=	ENSP00000486455.1:p.Cys78=
NM_024649.4:c.267T=	NP_078925.3:p.Ala89=
NM_024649.5:c.267T= MANE Select	NP_078925.3:p.Ala89=