Canonical Allele Identifier: CA381457228

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66282142C>T (hg19) ; chr11:g.66514671C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514671C>T , CM000673.2:g.66514671C>T	GRCh38
NC_000011.9:g.66282142C>T , CM000673.1:g.66282142C>T	GRCh37
NC_000011.8:g.66038718C>T	NCBI36
NG_009093.1:g.9024C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.425C>T MANE Select	ENSP00000317469.7:p.Ala142Val
ENST00000318312.11:c.425C>T	ENSP00000317469.7:p.Ala142Val
ENST00000393994.4:c.425C>T	ENSP00000377563.2:p.Ala142Val
ENST00000419755.3:c.536C>T	ENSP00000398526.3:p.Ala179Val
ENST00000455748.6:c.425C>T	ENSP00000405764.2:p.Ala142Val
ENST00000524458.5:c.*132C>T	ENSP00000436195.1:n.*132C>T
ENST00000524705.2:c.146C>T	ENSP00000436927.1:p.Ala49Val
ENST00000524907.5:n.415C>T
ENST00000525809.5:c.160-869C>T	ENSP00000431187.1:n.160-869C>T
ENST00000526035.5:c.*132C>T	ENSP00000434197.1:n.*132C>T
ENST00000526760.5:c.*132C>T	ENSP00000432140.1:n.*132C>T
ENST00000527251.5:c.*132C>T	ENSP00000434360.1:n.*132C>T
ENST00000529766.5:n.432C>T
ENST00000529953.5:n.77C>T
ENST00000529955.5:n.443C>T
ENST00000532908.5:c.*132C>T	ENSP00000431866.1:n.*132C>T
ENST00000533430.5:n.203C>T
ENST00000533557.5:c.*132C>T	ENSP00000434619.1:n.*132C>T
ENST00000533644.5:c.425C>T	ENSP00000436073.1:p.Ala142Val
ENST00000534730.5:n.437C>T
ENST00000630659.2:c.*132C>T	ENSP00000486455.1:n.*132C>T
NM_024649.4:c.425C>T	NP_078925.3:p.Ala142Val
NM_024649.5:c.425C>T MANE Select	NP_078925.3:p.Ala142Val