Canonical Allele Identifier: CA381457351
Gene: BBS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515570A>T , CM000673.2:g.66515570A>T GRCh38
NC_000011.9:g.66283041A>T , CM000673.1:g.66283041A>T GRCh37
NC_000011.8:g.66039617A>T NCBI36
NG_009093.1:g.9923A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.463A>T MANE Select ENSP00000317469.7:p.Met155Leu
ENST00000318312.11:c.463A>T ENSP00000317469.7:p.Met155Leu
ENST00000393994.4:c.463A>T ENSP00000377563.2:p.Met155Leu
ENST00000419755.3:c.574A>T ENSP00000398526.3:p.Met192Leu
ENST00000455748.6:c.432+892A>T ENSP00000405764.2:n.432+892A>T
ENST00000524458.5:c.*140-123A>T ENSP00000436195.1:n.*140-123A>T
ENST00000524705.2:c.184A>T ENSP00000436927.1:p.Met62Leu
ENST00000524907.5:n.453A>T
ENST00000525809.5:c.190A>T ENSP00000431187.1:p.Met64Leu
ENST00000526035.5:c.*170A>T ENSP00000434197.1:n.*170A>T
ENST00000526760.5:c.*170A>T ENSP00000432140.1:n.*170A>T
ENST00000527251.5:c.*170A>T ENSP00000434360.1:n.*170A>T
ENST00000529766.5:n.470A>T
ENST00000529953.5:n.115A>T
ENST00000529955.5:n.451-123A>T
ENST00000532908.5:c.*140-123A>T ENSP00000431866.1:n.*140-123A>T
ENST00000533430.5:n.241A>T
ENST00000533557.5:c.*140-123A>T ENSP00000434619.1:n.*140-123A>T
ENST00000533644.5:c.433-123A>T ENSP00000436073.1:n.433-123A>T
ENST00000534730.5:n.475A>T
ENST00000630659.2:c.*170A>T ENSP00000486455.1:n.*170A>T
NM_024649.4:c.463A>T NP_078925.3:p.Met155Leu
NM_024649.5:c.463A>T MANE Select NP_078925.3:p.Met155Leu