Canonical Allele Identifier: CA2499221202

Gene: BBS1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515943C>A , CM000673.2:g.66515943C>A	GRCh38
NC_000011.9:g.66283414C>A , CM000673.1:g.66283414C>A	GRCh37
NC_000011.8:g.66039990C>A	NCBI36
NG_009093.1:g.10296C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.591+10C>A MANE Select	ENSP00000317469.7:n.591+10C>A
ENST00000318312.11:c.591+10C>A	ENSP00000317469.7:n.591+10C>A
ENST00000393994.4:c.591+10C>A	ENSP00000377563.2:n.591+10C>A
ENST00000419755.3:c.702+10C>A	ENSP00000398526.3:n.702+10C>A
ENST00000455748.6:c.432+1265C>A	ENSP00000405764.2:n.432+1265C>A
ENST00000524458.5:c.*380+10C>A	ENSP00000436195.1:n.*380+10C>A
ENST00000524907.5:n.687+10C>A
ENST00000525809.5:c.318+10C>A	ENSP00000431187.1:n.318+10C>A
ENST00000526035.5:c.*298+10C>A	ENSP00000434197.1:n.*298+10C>A
ENST00000526760.5:c.*298+10C>A	ENSP00000432140.1:n.*298+10C>A
ENST00000527251.5:c.*298+10C>A	ENSP00000434360.1:n.*298+10C>A
ENST00000528543.1:n.113+10C>A
ENST00000529766.5:n.598+10C>A
ENST00000529953.5:n.243+10C>A
ENST00000529955.5:n.562+10C>A
ENST00000532908.5:c.*251+10C>A	ENSP00000431866.1:n.*251+10C>A
ENST00000533430.5:n.369+10C>A
ENST00000533557.5:c.*251+10C>A	ENSP00000434619.1:n.*251+10C>A
ENST00000533644.5:c.*49+10C>A	ENSP00000436073.1:n.*49+10C>A
ENST00000630659.2:c.*298+10C>A	ENSP00000486455.1:n.*298+10C>A
NM_024649.4:c.591+10C>A	NP_078925.3:n.591+10C>A
NM_024649.5:c.591+10C>A MANE Select	NP_078925.3:n.591+10C>A