Canonical Allele Identifier: CA1979716662
Gene: BBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514492A= , CM000673.2:g.66514492A= GRCh38
NC_000011.9:g.66281963A= , CM000673.1:g.66281963A= GRCh37
NC_000011.8:g.66038539A= NCBI36
NG_009093.1:g.8845A=

Transcript Alleles

HGVS Amino-acid change
ENST00000318312.12:c.246A= MANE Select ENSP00000317469.7:p.Leu82=
ENST00000318312.11:c.246A= ENSP00000317469.7:p.Leu82=
ENST00000393994.4:c.246A= ENSP00000377563.2:p.Leu82=
ENST00000419755.3:c.357A= ENSP00000398526.3:p.Leu119=
ENST00000455748.6:c.246A= ENSP00000405764.2:p.Leu82=
ENST00000524458.5:c.121A= ENSP00000436195.1:p.Thr41=
ENST00000524705.2:c.-20-14A= ENSP00000436927.1:n.-20-14A=
ENST00000524907.5:n.236A=
ENST00000525809.5:c.160-1048A= ENSP00000431187.1:n.160-1048A=
ENST00000526035.5:c.211A= ENSP00000434197.1:p.Thr71=
ENST00000526760.5:c.211A= ENSP00000432140.1:p.Thr71=
ENST00000526815.5:c.156A= ENSP00000436860.1:p.Leu52=
ENST00000527251.5:c.121A= ENSP00000434360.1:p.Thr41=
ENST00000529766.5:n.253A=
ENST00000529955.5:n.264A=
ENST00000532908.5:c.211A= ENSP00000431866.1:p.Thr71=
ENST00000533430.5:n.24A=
ENST00000533557.5:c.211A= ENSP00000434619.1:p.Thr71=
ENST00000533644.5:c.246A= ENSP00000436073.1:p.Leu82=
ENST00000534730.5:n.258A=
ENST00000630659.2:c.211A= ENSP00000486455.1:p.Thr71=
NM_024649.4:c.246A= NP_078925.3:p.Leu82=
NM_024649.5:c.246A= MANE Select NP_078925.3:p.Leu82=