Canonical Allele Identifier: CA381456165

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66281961C>A (hg19) ; chr11:g.66514490C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514490C>A , CM000673.2:g.66514490C>A	GRCh38
NC_000011.9:g.66281961C>A , CM000673.1:g.66281961C>A	GRCh37
NC_000011.8:g.66038537C>A	NCBI36
NG_009093.1:g.8843C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.244C>A MANE Select	ENSP00000317469.7:p.Leu82Ile
ENST00000318312.11:c.244C>A	ENSP00000317469.7:p.Leu82Ile
ENST00000393994.4:c.244C>A	ENSP00000377563.2:p.Leu82Ile
ENST00000419755.3:c.355C>A	ENSP00000398526.3:p.Leu119Ile
ENST00000455748.6:c.244C>A	ENSP00000405764.2:p.Leu82Ile
ENST00000524458.5:c.119C>A	ENSP00000436195.1:p.Ala40Asp
ENST00000524705.2:c.-20-16C>A	ENSP00000436927.1:n.-20-16C>A
ENST00000524907.5:n.234C>A
ENST00000525809.5:c.160-1050C>A	ENSP00000431187.1:n.160-1050C>A
ENST00000526035.5:c.209C>A	ENSP00000434197.1:p.Ala70Asp
ENST00000526760.5:c.209C>A	ENSP00000432140.1:p.Ala70Asp
ENST00000526815.5:c.154C>A	ENSP00000436860.1:p.Leu52Ile
ENST00000527251.5:c.119C>A	ENSP00000434360.1:p.Ala40Asp
ENST00000529766.5:n.251C>A
ENST00000529955.5:n.262C>A
ENST00000532908.5:c.209C>A	ENSP00000431866.1:p.Ala70Asp
ENST00000533430.5:n.22C>A
ENST00000533557.5:c.209C>A	ENSP00000434619.1:p.Ala70Asp
ENST00000533644.5:c.244C>A	ENSP00000436073.1:p.Leu82Ile
ENST00000534730.5:n.256C>A
ENST00000630659.2:c.209C>A	ENSP00000486455.1:p.Ala70Asp
NM_024649.4:c.244C>A	NP_078925.3:p.Leu82Ile
NM_024649.5:c.244C>A MANE Select	NP_078925.3:p.Leu82Ile