Canonical Allele Identifier: CA2614499070
Gene: BBS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515794del , CM000673.2:g.66515794del GRCh38
NC_000011.9:g.66283265del , CM000673.1:g.66283265del GRCh37
NC_000011.8:g.66039841del NCBI36
NG_009093.1:g.10147del

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.518+63del MANE Select ENSP00000317469.7:n.518+63del
ENST00000318312.11:c.518+63del ENSP00000317469.7:n.518+63del
ENST00000393994.4:c.518+63del ENSP00000377563.2:n.518+63del
ENST00000419755.3:c.629+63del ENSP00000398526.3:n.629+63del
ENST00000455748.6:c.432+1116del ENSP00000405764.2:n.432+1116del
ENST00000524458.5:c.*241del ENSP00000436195.1:n.*241del
ENST00000524907.5:n.614+63del
ENST00000525809.5:c.245+63del ENSP00000431187.1:n.245+63del
ENST00000526035.5:c.*225+63del ENSP00000434197.1:n.*225+63del
ENST00000526760.5:c.*225+63del ENSP00000432140.1:n.*225+63del
ENST00000527251.5:c.*225+63del ENSP00000434360.1:n.*225+63del
ENST00000528543.1:n.40+63del
ENST00000529766.5:n.525+63del
ENST00000529953.5:n.170+63del
ENST00000529955.5:n.489+63del
ENST00000532908.5:c.*178+63del ENSP00000431866.1:n.*178+63del
ENST00000533430.5:n.296+63del
ENST00000533557.5:c.*178+63del ENSP00000434619.1:n.*178+63del
ENST00000533644.5:c.471+63del ENSP00000436073.1:n.471+63del
ENST00000534730.5:n.593del
ENST00000630659.2:c.*225+63del ENSP00000486455.1:n.*225+63del
NM_024649.4:c.518+63del NP_078925.3:n.518+63del
NM_024649.5:c.518+63del MANE Select NP_078925.3:n.518+63del