Canonical Allele Identifier: CA475368283
Gene: BBS1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510704G>A , CM000673.2:g.66510704G>A GRCh38
NC_000011.9:g.66278175G>A , CM000673.1:g.66278175G>A GRCh37
NC_000011.8:g.66034751G>A NCBI36
NG_009093.1:g.5057G>A
NG_032068.1:g.35296G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.45G>A MANE Select ENSP00000317469.7:p.Glu15=
ENST00000318312.11:c.45G>A ENSP00000317469.7:p.Glu15=
ENST00000393994.4:c.45G>A ENSP00000377563.2:p.Glu15=
ENST00000419755.3:c.159-309G>A ENSP00000398526.3:n.159-309G>A
ENST00000455748.6:c.45G>A ENSP00000405764.2:p.Glu15=
ENST00000524907.5:n.35G>A
ENST00000525809.5:c.45G>A ENSP00000431187.1:p.Glu15=
ENST00000526035.5:c.45G>A ENSP00000434197.1:p.Glu15=
ENST00000526760.5:c.45G>A ENSP00000432140.1:p.Glu15=
ENST00000526815.5:c.-352G>A ENSP00000436860.1:n.-352G>A
ENST00000527251.5:c.-352G>A ENSP00000434360.1:n.-352G>A
ENST00000529766.5:n.52G>A
ENST00000529955.5:n.63G>A
ENST00000532908.5:c.45G>A ENSP00000431866.1:p.Glu15=
ENST00000533557.5:c.45G>A ENSP00000434619.1:p.Glu15=
ENST00000533644.5:c.45G>A ENSP00000436073.1:p.Glu15=
ENST00000534730.5:n.57G>A
ENST00000630659.2:c.45G>A ENSP00000486455.1:p.Glu15=
NM_024649.4:c.45G>A NP_078925.3:p.Glu15=
NM_024649.5:c.45G>A MANE Select NP_078925.3:p.Glu15=