Canonical Allele Identifier: CA2840488868

Gene: BBS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515684dup , CM000673.2:g.66515684dup	GRCh38
NC_000011.9:g.66283155dup , CM000673.1:g.66283155dup	GRCh37
NC_000011.8:g.66039731dup	NCBI36
NG_009093.1:g.10037dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.480-9dup MANE Select	ENSP00000317469.7:n.480-9dup
ENST00000318312.11:c.480-9dup	ENSP00000317469.7:n.480-9dup
ENST00000393994.4:c.480-9dup	ENSP00000377563.2:n.480-9dup
ENST00000419755.3:c.591-9dup	ENSP00000398526.3:n.591-9dup
ENST00000455748.6:c.432+1006dup	ENSP00000405764.2:n.432+1006dup
ENST00000524458.5:c.*140-9dup	ENSP00000436195.1:n.*140-9dup
ENST00000524907.5:n.567dup
ENST00000525809.5:c.207-9dup	ENSP00000431187.1:n.207-9dup
ENST00000526035.5:c.*187-9dup	ENSP00000434197.1:n.*187-9dup
ENST00000526760.5:c.*187-9dup	ENSP00000432140.1:n.*187-9dup
ENST00000527251.5:c.*187-9dup	ENSP00000434360.1:n.*187-9dup
ENST00000529766.5:n.487-9dup
ENST00000529953.5:n.132-9dup
ENST00000529955.5:n.451-9dup
ENST00000532908.5:c.*140-9dup	ENSP00000431866.1:n.*140-9dup
ENST00000533430.5:n.258-9dup
ENST00000533557.5:c.*140-9dup	ENSP00000434619.1:n.*140-9dup
ENST00000533644.5:c.433-9dup	ENSP00000436073.1:n.433-9dup
ENST00000534730.5:n.492-9dup
ENST00000630659.2:c.*187-9dup	ENSP00000486455.1:n.*187-9dup
NM_024649.4:c.480-9dup	NP_078925.3:n.480-9dup
NM_024649.5:c.480-9dup MANE Select	NP_078925.3:n.480-9dup