Canonical Allele Identifier: CA2614499068
Gene: BBS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515796_66515805del , CM000673.2:g.66515796_66515805del GRCh38
NC_000011.9:g.66283267_66283276del , CM000673.1:g.66283267_66283276del GRCh37
NC_000011.8:g.66039843_66039852del NCBI36
NG_009093.1:g.10149_10158del

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.519-65_519-56del MANE Select ENSP00000317469.7:n.519-65_519-56del
ENST00000318312.11:c.519-65_519-56del ENSP00000317469.7:n.519-65_519-56del
ENST00000393994.4:c.519-65_519-56del ENSP00000377563.2:n.519-65_519-56del
ENST00000419755.3:c.630-65_630-56del ENSP00000398526.3:n.630-65_630-56del
ENST00000455748.6:c.432+1118_432+1127del ENSP00000405764.2:n.432+1118_432+1127del
ENST00000524458.5:c.*243_*252del ENSP00000436195.1:n.*243_*252del
ENST00000524907.5:n.615-65_615-56del
ENST00000525809.5:c.246-65_246-56del ENSP00000431187.1:n.246-65_246-56del
ENST00000526035.5:c.*226-65_*226-56del ENSP00000434197.1:n.*226-65_*226-56del
ENST00000526760.5:c.*226-65_*226-56del ENSP00000432140.1:n.*226-65_*226-56del
ENST00000527251.5:c.*226-65_*226-56del ENSP00000434360.1:n.*226-65_*226-56del
ENST00000528543.1:n.41-65_41-56del
ENST00000529766.5:n.526-65_526-56del
ENST00000529953.5:n.171-65_171-56del
ENST00000529955.5:n.490-65_490-56del
ENST00000532908.5:c.*179-65_*179-56del ENSP00000431866.1:n.*179-65_*179-56del
ENST00000533430.5:n.297-65_297-56del
ENST00000533557.5:c.*179-65_*179-56del ENSP00000434619.1:n.*179-65_*179-56del
ENST00000533644.5:c.472-65_472-56del ENSP00000436073.1:n.472-65_472-56del
ENST00000534730.5:n.595_604del
ENST00000630659.2:c.*226-65_*226-56del ENSP00000486455.1:n.*226-65_*226-56del
NM_024649.4:c.519-65_519-56del NP_078925.3:n.519-65_519-56del
NM_024649.5:c.519-65_519-56del MANE Select NP_078925.3:n.519-65_519-56del