Canonical Allele Identifier: CA381456037
Gene: BBS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514476T>G , CM000673.2:g.66514476T>G GRCh38
NC_000011.9:g.66281947T>G , CM000673.1:g.66281947T>G GRCh37
NC_000011.8:g.66038523T>G NCBI36
NG_009093.1:g.8829T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.230T>G MANE Select ENSP00000317469.7:p.Met77Arg
ENST00000318312.11:c.230T>G ENSP00000317469.7:p.Met77Arg
ENST00000393994.4:c.230T>G ENSP00000377563.2:p.Met77Arg
ENST00000419755.3:c.341T>G ENSP00000398526.3:p.Met114Arg
ENST00000455748.6:c.230T>G ENSP00000405764.2:p.Met77Arg
ENST00000524458.5:c.105T>G ENSP00000436195.1:p.Asp35Glu
ENST00000524705.2:c.-20-30T>G ENSP00000436927.1:n.-20-30T>G
ENST00000524907.5:n.220T>G
ENST00000525809.5:c.160-1064T>G ENSP00000431187.1:n.160-1064T>G
ENST00000526035.5:c.195T>G ENSP00000434197.1:p.Asp65Glu
ENST00000526760.5:c.195T>G ENSP00000432140.1:p.Asp65Glu
ENST00000526815.5:c.140T>G ENSP00000436860.1:p.Met47Arg
ENST00000527251.5:c.105T>G ENSP00000434360.1:p.Asp35Glu
ENST00000529766.5:n.237T>G
ENST00000529955.5:n.248T>G
ENST00000532908.5:c.195T>G ENSP00000431866.1:p.Asp65Glu
ENST00000533430.5:n.8T>G
ENST00000533557.5:c.195T>G ENSP00000434619.1:p.Asp65Glu
ENST00000533644.5:c.230T>G ENSP00000436073.1:p.Met77Arg
ENST00000534730.5:n.242T>G
ENST00000630659.2:c.195T>G ENSP00000486455.1:p.Asp65Glu
NM_024649.4:c.230T>G NP_078925.3:p.Met77Arg
NM_024649.5:c.230T>G MANE Select NP_078925.3:p.Met77Arg