Canonical Allele Identifier: CA1979716832
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514575C= , CM000673.2:g.66514575C= GRCh38
NC_000011.9:g.66282046C= , CM000673.1:g.66282046C= GRCh37
NC_000011.8:g.66038622C= NCBI36
NG_009093.1:g.8928C=

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.329C= MANE Select ENSP00000317469.7:p.Pro110=
ENST00000318312.11:c.329C= ENSP00000317469.7:p.Pro110=
ENST00000393994.4:c.329C= ENSP00000377563.2:p.Pro110=
ENST00000419755.3:c.440C= ENSP00000398526.3:p.Pro147=
ENST00000455748.6:c.329C= ENSP00000405764.2:p.Pro110=
ENST00000524458.5:c.*36C= ENSP00000436195.1:n.*36C=
ENST00000524705.2:c.50C= ENSP00000436927.1:p.Pro17=
ENST00000524907.5:n.319C=
ENST00000525809.5:c.160-965C= ENSP00000431187.1:n.160-965C=
ENST00000526035.5:c.*36C= ENSP00000434197.1:n.*36C=
ENST00000526760.5:c.*36C= ENSP00000432140.1:n.*36C=
ENST00000527251.5:c.*36C= ENSP00000434360.1:n.*36C=
ENST00000529766.5:n.336C=
ENST00000529955.5:n.347C=
ENST00000532908.5:c.*36C= ENSP00000431866.1:n.*36C=
ENST00000533430.5:n.107C=
ENST00000533557.5:c.*36C= ENSP00000434619.1:n.*36C=
ENST00000533644.5:c.329C= ENSP00000436073.1:p.Pro110=
ENST00000534730.5:n.341C=
ENST00000630659.2:c.*36C= ENSP00000486455.1:n.*36C=
NM_024649.4:c.329C= NP_078925.3:p.Pro110=
NM_024649.5:c.329C= MANE Select NP_078925.3:p.Pro110=