Canonical Allele Identifier: CA381456353

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66281989C>G (hg19) ; chr11:g.66514518C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514518C>G , CM000673.2:g.66514518C>G	GRCh38
NC_000011.9:g.66281989C>G , CM000673.1:g.66281989C>G	GRCh37
NC_000011.8:g.66038565C>G	NCBI36
NG_009093.1:g.8871C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.272C>G MANE Select	ENSP00000317469.7:p.Thr91Ser
ENST00000318312.11:c.272C>G	ENSP00000317469.7:p.Thr91Ser
ENST00000393994.4:c.272C>G	ENSP00000377563.2:p.Thr91Ser
ENST00000419755.3:c.383C>G	ENSP00000398526.3:p.Thr128Ser
ENST00000455748.6:c.272C>G	ENSP00000405764.2:p.Thr91Ser
ENST00000524458.5:c.147C>G	ENSP00000436195.1:p.His49Gln
ENST00000524705.2:c.-8C>G	ENSP00000436927.1:n.-8C>G
ENST00000524907.5:n.262C>G
ENST00000525809.5:c.160-1022C>G	ENSP00000431187.1:n.160-1022C>G
ENST00000526035.5:c.237C>G	ENSP00000434197.1:p.His79Gln
ENST00000526760.5:c.237C>G	ENSP00000432140.1:p.His79Gln
ENST00000527251.5:c.147C>G	ENSP00000434360.1:p.His49Gln
ENST00000529766.5:n.279C>G
ENST00000529955.5:n.290C>G
ENST00000532908.5:c.237C>G	ENSP00000431866.1:p.His79Gln
ENST00000533430.5:n.50C>G
ENST00000533557.5:c.237C>G	ENSP00000434619.1:p.His79Gln
ENST00000533644.5:c.272C>G	ENSP00000436073.1:p.Thr91Ser
ENST00000534730.5:n.284C>G
ENST00000630659.2:c.237C>G	ENSP00000486455.1:p.His79Gln
NM_024649.4:c.272C>G	NP_078925.3:p.Thr91Ser
NM_024649.5:c.272C>G MANE Select	NP_078925.3:p.Thr91Ser