Canonical Allele Identifier: CA1979717017
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514673A= , CM000673.2:g.66514673A= GRCh38
NC_000011.9:g.66282144A= , CM000673.1:g.66282144A= GRCh37
NC_000011.8:g.66038720A= NCBI36
NG_009093.1:g.9026A=

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.427A= MANE Select ENSP00000317469.7:p.Lys143=
ENST00000318312.11:c.427A= ENSP00000317469.7:p.Lys143=
ENST00000393994.4:c.427A= ENSP00000377563.2:p.Lys143=
ENST00000419755.3:c.538A= ENSP00000398526.3:p.Lys180=
ENST00000455748.6:c.427A= ENSP00000405764.2:p.Lys143=
ENST00000524458.5:c.*134A= ENSP00000436195.1:n.*134A=
ENST00000524705.2:c.148A= ENSP00000436927.1:p.Lys50=
ENST00000524907.5:n.417A=
ENST00000525809.5:c.160-867A= ENSP00000431187.1:n.160-867A=
ENST00000526035.5:c.*134A= ENSP00000434197.1:n.*134A=
ENST00000526760.5:c.*134A= ENSP00000432140.1:n.*134A=
ENST00000527251.5:c.*134A= ENSP00000434360.1:n.*134A=
ENST00000529766.5:n.434A=
ENST00000529953.5:n.79A=
ENST00000529955.5:n.445A=
ENST00000532908.5:c.*134A= ENSP00000431866.1:n.*134A=
ENST00000533430.5:n.205A=
ENST00000533557.5:c.*134A= ENSP00000434619.1:n.*134A=
ENST00000533644.5:c.427A= ENSP00000436073.1:p.Lys143=
ENST00000534730.5:n.439A=
ENST00000630659.2:c.*134A= ENSP00000486455.1:n.*134A=
NM_024649.4:c.427A= NP_078925.3:p.Lys143=
NM_024649.5:c.427A= MANE Select NP_078925.3:p.Lys143=