Canonical Allele Identifier: CA1979712011
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510645A= , CM000673.2:g.66510645A= GRCh38
NC_000011.9:g.66278116A= , CM000673.1:g.66278116A= GRCh37
NC_000011.8:g.66034692A= NCBI36
NG_009093.1:g.4998A=
NG_032068.1:g.35237A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.-15A= MANE Select ENSP00000317469.7:n.-15A=
ENST00000318312.11:c.-15A= ENSP00000317469.7:n.-15A=
ENST00000419755.3:c.159-368A= ENSP00000398526.3:n.159-368A=
ENST00000455748.6:c.-15A= ENSP00000405764.2:n.-15A=
ENST00000525809.5:c.-15A= ENSP00000431187.1:n.-15A=
ENST00000526035.5:c.-15A= ENSP00000434197.1:n.-15A=
ENST00000526760.5:c.-15A= ENSP00000432140.1:n.-15A=
ENST00000526815.5:c.-411A= ENSP00000436860.1:n.-411A=
ENST00000527251.5:c.-411A= ENSP00000434360.1:n.-411A=
ENST00000529955.5:n.4A=
ENST00000533557.5:c.-15A= ENSP00000434619.1:n.-15A=
ENST00000533644.5:c.-15A= ENSP00000436073.1:n.-15A=
NM_024649.5:c.-15A= MANE Select NP_078925.3:n.-15A=