Canonical Allele Identifier: CA679423129

Gene: BBS1

Linked Data

• dbSNP Id: rs1462355570
• MyVariant Identifiers: chr11:g.66283086_66283087insG (hg19) ; chr11:g.66515615_66515616insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515615_66515616insG , CM000673.2:g.66515615_66515616insG	GRCh38
NC_000011.9:g.66283086_66283087insG , CM000673.1:g.66283086_66283087insG	GRCh37
NC_000011.8:g.66039662_66039663insG	NCBI36
NG_009093.1:g.9968_9969insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.479+29_479+30insG MANE Select	ENSP00000317469.7:n.479+29_479+30insG
ENST00000318312.11:c.479+29_479+30insG	ENSP00000317469.7:n.479+29_479+30insG
ENST00000393994.4:c.479+29_479+30insG	ENSP00000377563.2:n.479+29_479+30insG
ENST00000419755.3:c.590+29_590+30insG	ENSP00000398526.3:n.590+29_590+30insG
ENST00000455748.6:c.432+937_432+938insG	ENSP00000405764.2:n.432+937_432+938insG
ENST00000524458.5:c.*140-78_*140-77insG	ENSP00000436195.1:n.*140-78_*140-77insG
ENST00000524907.5:n.498_499insG
ENST00000525809.5:c.206+29_206+30insG	ENSP00000431187.1:n.206+29_206+30insG
ENST00000526035.5:c.*186+29_*186+30insG	ENSP00000434197.1:n.*186+29_*186+30insG
ENST00000526760.5:c.*186+29_*186+30insG	ENSP00000432140.1:n.*186+29_*186+30insG
ENST00000527251.5:c.*186+29_*186+30insG	ENSP00000434360.1:n.*186+29_*186+30insG
ENST00000529766.5:n.486+29_486+30insG
ENST00000529953.5:n.131+29_131+30insG
ENST00000529955.5:n.451-78_451-77insG
ENST00000532908.5:c.*140-78_*140-77insG	ENSP00000431866.1:n.*140-78_*140-77insG
ENST00000533430.5:n.257+29_257+30insG
ENST00000533557.5:c.*140-78_*140-77insG	ENSP00000434619.1:n.*140-78_*140-77insG
ENST00000533644.5:c.433-78_433-77insG	ENSP00000436073.1:n.433-78_433-77insG
ENST00000534730.5:n.491+29_491+30insG
ENST00000630659.2:c.*186+29_*186+30insG	ENSP00000486455.1:n.*186+29_*186+30insG
NM_024649.4:c.479+29_479+30insG	NP_078925.3:n.479+29_479+30insG
NM_024649.5:c.479+29_479+30insG MANE Select	NP_078925.3:n.479+29_479+30insG