Canonical Allele Identifier: CA381455926
Gene: BBS1 HGNC NCBI

Linked Data

dbSNP Id: rs1856007963

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514460A>G , CM000673.2:g.66514460A>G GRCh38
NC_000011.9:g.66281931A>G , CM000673.1:g.66281931A>G GRCh37
NC_000011.8:g.66038507A>G NCBI36
NG_009093.1:g.8813A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.214A>G MANE Select ENSP00000317469.7:p.Lys72Glu
ENST00000318312.11:c.214A>G ENSP00000317469.7:p.Lys72Glu
ENST00000393994.4:c.214A>G ENSP00000377563.2:p.Lys72Glu
ENST00000419755.3:c.325A>G ENSP00000398526.3:p.Lys109Glu
ENST00000455748.6:c.214A>G ENSP00000405764.2:p.Lys72Glu
ENST00000524458.5:c.89A>G ENSP00000436195.1:p.Gln30Arg
ENST00000524705.2:c.-20-46A>G ENSP00000436927.1:n.-20-46A>G
ENST00000524907.5:n.204A>G
ENST00000525809.5:c.160-1080A>G ENSP00000431187.1:n.160-1080A>G
ENST00000526035.5:c.179A>G ENSP00000434197.1:p.Gln60Arg
ENST00000526760.5:c.179A>G ENSP00000432140.1:p.Gln60Arg
ENST00000526815.5:c.124A>G ENSP00000436860.1:p.Lys42Glu
ENST00000527251.5:c.89A>G ENSP00000434360.1:p.Gln30Arg
ENST00000529766.5:n.221A>G
ENST00000529955.5:n.232A>G
ENST00000532908.5:c.179A>G ENSP00000431866.1:p.Gln60Arg
ENST00000533557.5:c.179A>G ENSP00000434619.1:p.Gln60Arg
ENST00000533644.5:c.214A>G ENSP00000436073.1:p.Lys72Glu
ENST00000534730.5:n.226A>G
ENST00000630659.2:c.179A>G ENSP00000486455.1:p.Gln60Arg
NM_024649.4:c.214A>G NP_078925.3:p.Lys72Glu
NM_024649.5:c.214A>G MANE Select NP_078925.3:p.Lys72Glu