Canonical Allele Identifier: CA381456068
Gene: BBS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514479C>G , CM000673.2:g.66514479C>G GRCh38
NC_000011.9:g.66281950C>G , CM000673.1:g.66281950C>G GRCh37
NC_000011.8:g.66038526C>G NCBI36
NG_009093.1:g.8832C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.233C>G MANE Select ENSP00000317469.7:p.Thr78Ser
ENST00000318312.11:c.233C>G ENSP00000317469.7:p.Thr78Ser
ENST00000393994.4:c.233C>G ENSP00000377563.2:p.Thr78Ser
ENST00000419755.3:c.344C>G ENSP00000398526.3:p.Thr115Ser
ENST00000455748.6:c.233C>G ENSP00000405764.2:p.Thr78Ser
ENST00000524458.5:c.108C>G ENSP00000436195.1:p.Asp36Glu
ENST00000524705.2:c.-20-27C>G ENSP00000436927.1:n.-20-27C>G
ENST00000524907.5:n.223C>G
ENST00000525809.5:c.160-1061C>G ENSP00000431187.1:n.160-1061C>G
ENST00000526035.5:c.198C>G ENSP00000434197.1:p.Asp66Glu
ENST00000526760.5:c.198C>G ENSP00000432140.1:p.Asp66Glu
ENST00000526815.5:c.143C>G ENSP00000436860.1:p.Thr48Ser
ENST00000527251.5:c.108C>G ENSP00000434360.1:p.Asp36Glu
ENST00000529766.5:n.240C>G
ENST00000529955.5:n.251C>G
ENST00000532908.5:c.198C>G ENSP00000431866.1:p.Asp66Glu
ENST00000533430.5:n.11C>G
ENST00000533557.5:c.198C>G ENSP00000434619.1:p.Asp66Glu
ENST00000533644.5:c.233C>G ENSP00000436073.1:p.Thr78Ser
ENST00000534730.5:n.245C>G
ENST00000630659.2:c.198C>G ENSP00000486455.1:p.Asp66Glu
NM_024649.4:c.233C>G NP_078925.3:p.Thr78Ser
NM_024649.5:c.233C>G MANE Select NP_078925.3:p.Thr78Ser