Canonical Allele Identifier: CA381457292

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66283013C>G (hg19) ; chr11:g.66515542C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515542C>G , CM000673.2:g.66515542C>G	GRCh38
NC_000011.9:g.66283013C>G , CM000673.1:g.66283013C>G	GRCh37
NC_000011.8:g.66039589C>G	NCBI36
NG_009093.1:g.9895C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.435C>G MANE Select	ENSP00000317469.7:p.Asp145Glu
ENST00000318312.11:c.435C>G	ENSP00000317469.7:p.Asp145Glu
ENST00000393994.4:c.435C>G	ENSP00000377563.2:p.Asp145Glu
ENST00000419755.3:c.546C>G	ENSP00000398526.3:p.Asp182Glu
ENST00000455748.6:c.432+864C>G	ENSP00000405764.2:n.432+864C>G
ENST00000524458.5:c.*140-151C>G	ENSP00000436195.1:n.*140-151C>G
ENST00000524705.2:c.156C>G	ENSP00000436927.1:p.Asp52Glu
ENST00000524907.5:n.425C>G
ENST00000525809.5:c.162C>G	ENSP00000431187.1:p.Asp54Glu
ENST00000526035.5:c.*142C>G	ENSP00000434197.1:n.*142C>G
ENST00000526760.5:c.*142C>G	ENSP00000432140.1:n.*142C>G
ENST00000527251.5:c.*142C>G	ENSP00000434360.1:n.*142C>G
ENST00000529766.5:n.442C>G
ENST00000529953.5:n.87C>G
ENST00000529955.5:n.451-151C>G
ENST00000532908.5:c.*140-151C>G	ENSP00000431866.1:n.*140-151C>G
ENST00000533430.5:n.213C>G
ENST00000533557.5:c.*140-151C>G	ENSP00000434619.1:n.*140-151C>G
ENST00000533644.5:c.433-151C>G	ENSP00000436073.1:n.433-151C>G
ENST00000534730.5:n.447C>G
ENST00000630659.2:c.*142C>G	ENSP00000486455.1:n.*142C>G
NM_024649.4:c.435C>G	NP_078925.3:p.Asp145Glu
NM_024649.5:c.435C>G MANE Select	NP_078925.3:p.Asp145Glu