Canonical Allele Identifier: CA475492251

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66282038T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514567T>C , CM000673.2:g.66514567T>C	GRCh38
NC_000011.9:g.66282038T>C , CM000673.1:g.66282038T>C	GRCh37
NC_000011.8:g.66038614T>C	NCBI36
NG_009093.1:g.8920T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.321T>C MANE Select	ENSP00000317469.7:p.Ala107=
ENST00000318312.11:c.321T>C	ENSP00000317469.7:p.Ala107=
ENST00000393994.4:c.321T>C	ENSP00000377563.2:p.Ala107=
ENST00000419755.3:c.432T>C	ENSP00000398526.3:p.Ala144=
ENST00000455748.6:c.321T>C	ENSP00000405764.2:p.Ala107=
ENST00000524458.5:c.*28T>C	ENSP00000436195.1:n.*28T>C
ENST00000524705.2:c.42T>C	ENSP00000436927.1:p.Ala14=
ENST00000524907.5:n.311T>C
ENST00000525809.5:c.160-973T>C	ENSP00000431187.1:n.160-973T>C
ENST00000526035.5:c.*28T>C	ENSP00000434197.1:n.*28T>C
ENST00000526760.5:c.*28T>C	ENSP00000432140.1:n.*28T>C
ENST00000527251.5:c.*28T>C	ENSP00000434360.1:n.*28T>C
ENST00000529766.5:n.328T>C
ENST00000529955.5:n.339T>C
ENST00000532908.5:c.*28T>C	ENSP00000431866.1:n.*28T>C
ENST00000533430.5:n.99T>C
ENST00000533557.5:c.*28T>C	ENSP00000434619.1:n.*28T>C
ENST00000533644.5:c.321T>C	ENSP00000436073.1:p.Ala107=
ENST00000534730.5:n.333T>C
ENST00000630659.2:c.*28T>C	ENSP00000486455.1:n.*28T>C
NM_024649.4:c.321T>C	NP_078925.3:p.Ala107=
NM_024649.5:c.321T>C MANE Select	NP_078925.3:p.Ala107=