Canonical Allele Identifier: CA475368263
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510677A>T , CM000673.2:g.66510677A>T GRCh38
NC_000011.9:g.66278148A>T , CM000673.1:g.66278148A>T GRCh37
NC_000011.8:g.66034724A>T NCBI36
NG_009093.1:g.5030A>T
NG_032068.1:g.35269A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.18A>T MANE Select ENSP00000317469.7:p.Ser6=
ENST00000318312.11:c.18A>T ENSP00000317469.7:p.Ser6=
ENST00000393994.4:c.18A>T ENSP00000377563.2:p.Ser6=
ENST00000419755.3:c.159-336A>T ENSP00000398526.3:n.159-336A>T
ENST00000455748.6:c.18A>T ENSP00000405764.2:p.Ser6=
ENST00000524907.5:n.8A>T
ENST00000525809.5:c.18A>T ENSP00000431187.1:p.Ser6=
ENST00000526035.5:c.18A>T ENSP00000434197.1:p.Ser6=
ENST00000526760.5:c.18A>T ENSP00000432140.1:p.Ser6=
ENST00000526815.5:c.-379A>T ENSP00000436860.1:n.-379A>T
ENST00000527251.5:c.-379A>T ENSP00000434360.1:n.-379A>T
ENST00000529766.5:n.25A>T
ENST00000529955.5:n.36A>T
ENST00000532908.5:c.18A>T ENSP00000431866.1:p.Ser6=
ENST00000533557.5:c.18A>T ENSP00000434619.1:p.Ser6=
ENST00000533644.5:c.18A>T ENSP00000436073.1:p.Ser6=
ENST00000534730.5:n.30A>T
ENST00000630659.2:c.18A>T ENSP00000486455.1:p.Ser6=
NM_024649.4:c.18A>T NP_078925.3:p.Ser6=
NM_024649.5:c.18A>T MANE Select NP_078925.3:p.Ser6=