Canonical Allele Identifier: CA938989517
Gene: BBS1 HGNC NCBI

Linked Data

dbSNP Id: rs1856029814

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515508A>T , CM000673.2:g.66515508A>T GRCh38
NC_000011.9:g.66282979A>T , CM000673.1:g.66282979A>T GRCh37
NC_000011.8:g.66039555A>T NCBI36
NG_009093.1:g.9861A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.433-32A>T MANE Select ENSP00000317469.7:n.433-32A>T
ENST00000318312.11:c.433-32A>T ENSP00000317469.7:n.433-32A>T
ENST00000393994.4:c.433-32A>T ENSP00000377563.2:n.433-32A>T
ENST00000419755.3:c.544-32A>T ENSP00000398526.3:n.544-32A>T
ENST00000455748.6:c.432+830A>T ENSP00000405764.2:n.432+830A>T
ENST00000524458.5:c.*140-185A>T ENSP00000436195.1:n.*140-185A>T
ENST00000524705.2:c.154-32A>T ENSP00000436927.1:n.154-32A>T
ENST00000524907.5:n.423-32A>T
ENST00000525809.5:c.160-32A>T ENSP00000431187.1:n.160-32A>T
ENST00000526035.5:c.*140-32A>T ENSP00000434197.1:n.*140-32A>T
ENST00000526760.5:c.*140-32A>T ENSP00000432140.1:n.*140-32A>T
ENST00000527251.5:c.*140-32A>T ENSP00000434360.1:n.*140-32A>T
ENST00000529766.5:n.440-32A>T
ENST00000529953.5:n.85-32A>T
ENST00000529955.5:n.451-185A>T
ENST00000532908.5:c.*140-185A>T ENSP00000431866.1:n.*140-185A>T
ENST00000533430.5:n.211-32A>T
ENST00000533557.5:c.*140-185A>T ENSP00000434619.1:n.*140-185A>T
ENST00000533644.5:c.433-185A>T ENSP00000436073.1:n.433-185A>T
ENST00000534730.5:n.445-32A>T
ENST00000630659.2:c.*140-32A>T ENSP00000486455.1:n.*140-32A>T
NM_024649.4:c.433-32A>T NP_078925.3:n.433-32A>T
NM_024649.5:c.433-32A>T MANE Select NP_078925.3:n.433-32A>T