Canonical Allele Identifier: CA1979718815
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66515780A= , CM000673.2:g.66515780A= GRCh38
NC_000011.9:g.66283251A= , CM000673.1:g.66283251A= GRCh37
NC_000011.8:g.66039827A= NCBI36
NG_009093.1:g.10133A=

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.518+49A= MANE Select ENSP00000317469.7:n.518+49A=
ENST00000318312.11:c.518+49A= ENSP00000317469.7:n.518+49A=
ENST00000393994.4:c.518+49A= ENSP00000377563.2:n.518+49A=
ENST00000419755.3:c.629+49A= ENSP00000398526.3:n.629+49A=
ENST00000455748.6:c.432+1102A= ENSP00000405764.2:n.432+1102A=
ENST00000524458.5:c.*227A= ENSP00000436195.1:n.*227A=
ENST00000524907.5:n.614+49A=
ENST00000525809.5:c.245+49A= ENSP00000431187.1:n.245+49A=
ENST00000526035.5:c.*225+49A= ENSP00000434197.1:n.*225+49A=
ENST00000526760.5:c.*225+49A= ENSP00000432140.1:n.*225+49A=
ENST00000527251.5:c.*225+49A= ENSP00000434360.1:n.*225+49A=
ENST00000528543.1:n.40+49A=
ENST00000529766.5:n.525+49A=
ENST00000529953.5:n.170+49A=
ENST00000529955.5:n.489+49A=
ENST00000532908.5:c.*178+49A= ENSP00000431866.1:n.*178+49A=
ENST00000533430.5:n.296+49A=
ENST00000533557.5:c.*178+49A= ENSP00000434619.1:n.*178+49A=
ENST00000533644.5:c.471+49A= ENSP00000436073.1:n.471+49A=
ENST00000534730.5:n.579A=
ENST00000630659.2:c.*225+49A= ENSP00000486455.1:n.*225+49A=
NM_024649.4:c.518+49A= NP_078925.3:n.518+49A=
NM_024649.5:c.518+49A= MANE Select NP_078925.3:n.518+49A=