Canonical Allele Identifier: CA1979712056

Gene: BBS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66510665C= , CM000673.2:g.66510665C=	GRCh38
NC_000011.9:g.66278136C= , CM000673.1:g.66278136C=	GRCh37
NC_000011.8:g.66034712C=	NCBI36
NG_009093.1:g.5018C=
NG_032068.1:g.35257C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.6C= MANE Select	ENSP00000317469.7:p.Ala2=
ENST00000318312.11:c.6C=	ENSP00000317469.7:p.Ala2=
ENST00000393994.4:c.6C=	ENSP00000377563.2:p.Ala2=
ENST00000419755.3:c.159-348C=	ENSP00000398526.3:n.159-348C=
ENST00000455748.6:c.6C=	ENSP00000405764.2:p.Ala2=
ENST00000525809.5:c.6C=	ENSP00000431187.1:p.Ala2=
ENST00000526035.5:c.6C=	ENSP00000434197.1:p.Ala2=
ENST00000526760.5:c.6C=	ENSP00000432140.1:p.Ala2=
ENST00000526815.5:c.-391C=	ENSP00000436860.1:n.-391C=
ENST00000527251.5:c.-391C=	ENSP00000434360.1:n.-391C=
ENST00000529766.5:n.13C=
ENST00000529955.5:n.24C=
ENST00000532908.5:c.6C=	ENSP00000431866.1:p.Ala2=
ENST00000533557.5:c.6C=	ENSP00000434619.1:p.Ala2=
ENST00000533644.5:c.6C=	ENSP00000436073.1:p.Ala2=
ENST00000534730.5:n.18C=
ENST00000630659.2:c.6C=	ENSP00000486455.1:p.Ala2=
NM_024649.4:c.6C=	NP_078925.3:p.Ala2=
NM_024649.5:c.6C= MANE Select	NP_078925.3:p.Ala2=