Canonical Allele Identifier: CA381455994
Gene: BBS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514471G>T , CM000673.2:g.66514471G>T GRCh38
NC_000011.9:g.66281942G>T , CM000673.1:g.66281942G>T GRCh37
NC_000011.8:g.66038518G>T NCBI36
NG_009093.1:g.8824G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.225G>T MANE Select ENSP00000317469.7:p.Leu75=
ENST00000318312.11:c.225G>T ENSP00000317469.7:p.Leu75=
ENST00000393994.4:c.225G>T ENSP00000377563.2:p.Leu75=
ENST00000419755.3:c.336G>T ENSP00000398526.3:p.Leu112=
ENST00000455748.6:c.225G>T ENSP00000405764.2:p.Leu75=
ENST00000524458.5:c.100G>T ENSP00000436195.1:p.Gly34Cys
ENST00000524705.2:c.-20-35G>T ENSP00000436927.1:n.-20-35G>T
ENST00000524907.5:n.215G>T
ENST00000525809.5:c.160-1069G>T ENSP00000431187.1:n.160-1069G>T
ENST00000526035.5:c.190G>T ENSP00000434197.1:p.Gly64Cys
ENST00000526760.5:c.190G>T ENSP00000432140.1:p.Gly64Cys
ENST00000526815.5:c.135G>T ENSP00000436860.1:p.Leu45=
ENST00000527251.5:c.100G>T ENSP00000434360.1:p.Gly34Cys
ENST00000529766.5:n.232G>T
ENST00000529955.5:n.243G>T
ENST00000532908.5:c.190G>T ENSP00000431866.1:p.Gly64Cys
ENST00000533430.5:n.3G>T
ENST00000533557.5:c.190G>T ENSP00000434619.1:p.Gly64Cys
ENST00000533644.5:c.225G>T ENSP00000436073.1:p.Leu75=
ENST00000534730.5:n.237G>T
ENST00000630659.2:c.190G>T ENSP00000486455.1:p.Gly64Cys
NM_024649.4:c.225G>T NP_078925.3:p.Leu75=
NM_024649.5:c.225G>T MANE Select NP_078925.3:p.Leu75=