Canonical Allele Identifier: CA381456338

Gene: BBS1

Linked Data

• ClinVar Variation Id: 1087653
• ClinVar RCV Id: RCV001405817
• dbSNP Id: rs2134771366
• MyVariant Identifiers: chr11:g.66281987C>T (hg19) ; chr11:g.66514516C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514516C>T , CM000673.2:g.66514516C>T	GRCh38
NC_000011.9:g.66281987C>T , CM000673.1:g.66281987C>T	GRCh37
NC_000011.8:g.66038563C>T	NCBI36
NG_009093.1:g.8869C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.270C>T MANE Select	ENSP00000317469.7:p.Ala90=
ENST00000318312.11:c.270C>T	ENSP00000317469.7:p.Ala90=
ENST00000393994.4:c.270C>T	ENSP00000377563.2:p.Ala90=
ENST00000419755.3:c.381C>T	ENSP00000398526.3:p.Ala127=
ENST00000455748.6:c.270C>T	ENSP00000405764.2:p.Ala90=
ENST00000524458.5:c.145C>T	ENSP00000436195.1:p.His49Tyr
ENST00000524705.2:c.-10C>T	ENSP00000436927.1:n.-10C>T
ENST00000524907.5:n.260C>T
ENST00000525809.5:c.160-1024C>T	ENSP00000431187.1:n.160-1024C>T
ENST00000526035.5:c.235C>T	ENSP00000434197.1:p.His79Tyr
ENST00000526760.5:c.235C>T	ENSP00000432140.1:p.His79Tyr
ENST00000527251.5:c.145C>T	ENSP00000434360.1:p.His49Tyr
ENST00000529766.5:n.277C>T
ENST00000529955.5:n.288C>T
ENST00000532908.5:c.235C>T	ENSP00000431866.1:p.His79Tyr
ENST00000533430.5:n.48C>T
ENST00000533557.5:c.235C>T	ENSP00000434619.1:p.His79Tyr
ENST00000533644.5:c.270C>T	ENSP00000436073.1:p.Ala90=
ENST00000534730.5:n.282C>T
ENST00000630659.2:c.235C>T	ENSP00000486455.1:p.His79Tyr
NM_024649.4:c.270C>T	NP_078925.3:p.Ala90=
NM_024649.5:c.270C>T MANE Select	NP_078925.3:p.Ala90=