Canonical Allele Identifier: CA381455934
Gene: BBS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66514461A>T , CM000673.2:g.66514461A>T GRCh38
NC_000011.9:g.66281932A>T , CM000673.1:g.66281932A>T GRCh37
NC_000011.8:g.66038508A>T NCBI36
NG_009093.1:g.8814A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318312.12:c.215A>T MANE Select ENSP00000317469.7:p.Lys72Ile
ENST00000318312.11:c.215A>T ENSP00000317469.7:p.Lys72Ile
ENST00000393994.4:c.215A>T ENSP00000377563.2:p.Lys72Ile
ENST00000419755.3:c.326A>T ENSP00000398526.3:p.Lys109Ile
ENST00000455748.6:c.215A>T ENSP00000405764.2:p.Lys72Ile
ENST00000524458.5:c.90A>T ENSP00000436195.1:p.Gln30His
ENST00000524705.2:c.-20-45A>T ENSP00000436927.1:n.-20-45A>T
ENST00000524907.5:n.205A>T
ENST00000525809.5:c.160-1079A>T ENSP00000431187.1:n.160-1079A>T
ENST00000526035.5:c.180A>T ENSP00000434197.1:p.Gln60His
ENST00000526760.5:c.180A>T ENSP00000432140.1:p.Gln60His
ENST00000526815.5:c.125A>T ENSP00000436860.1:p.Lys42Ile
ENST00000527251.5:c.90A>T ENSP00000434360.1:p.Gln30His
ENST00000529766.5:n.222A>T
ENST00000529955.5:n.233A>T
ENST00000532908.5:c.180A>T ENSP00000431866.1:p.Gln60His
ENST00000533557.5:c.180A>T ENSP00000434619.1:p.Gln60His
ENST00000533644.5:c.215A>T ENSP00000436073.1:p.Lys72Ile
ENST00000534730.5:n.227A>T
ENST00000630659.2:c.180A>T ENSP00000486455.1:p.Gln60His
NM_024649.4:c.215A>T NP_078925.3:p.Lys72Ile
NM_024649.5:c.215A>T MANE Select NP_078925.3:p.Lys72Ile