Canonical Allele Identifier: CA381457405

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66283166A>T (hg19) ; chr11:g.66515695A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66515695A>T , CM000673.2:g.66515695A>T	GRCh38
NC_000011.9:g.66283166A>T , CM000673.1:g.66283166A>T	GRCh37
NC_000011.8:g.66039742A>T	NCBI36
NG_009093.1:g.10048A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318312.12:c.482A>T MANE Select	ENSP00000317469.7:p.Glu161Val
ENST00000318312.11:c.482A>T	ENSP00000317469.7:p.Glu161Val
ENST00000393994.4:c.482A>T	ENSP00000377563.2:p.Glu161Val
ENST00000419755.3:c.593A>T	ENSP00000398526.3:p.Glu198Val
ENST00000455748.6:c.432+1017A>T	ENSP00000405764.2:n.432+1017A>T
ENST00000524458.5:c.*142A>T	ENSP00000436195.1:n.*142A>T
ENST00000524907.5:n.578A>T
ENST00000525809.5:c.209A>T	ENSP00000431187.1:p.Glu70Val
ENST00000526035.5:c.*189A>T	ENSP00000434197.1:n.*189A>T
ENST00000526760.5:c.*189A>T	ENSP00000432140.1:n.*189A>T
ENST00000527251.5:c.*189A>T	ENSP00000434360.1:n.*189A>T
ENST00000528543.1:n.4A>T
ENST00000529766.5:n.489A>T
ENST00000529953.5:n.134A>T
ENST00000529955.5:n.453A>T
ENST00000532908.5:c.*142A>T	ENSP00000431866.1:n.*142A>T
ENST00000533430.5:n.260A>T
ENST00000533557.5:c.*142A>T	ENSP00000434619.1:n.*142A>T
ENST00000533644.5:c.435A>T	ENSP00000436073.1:p.Gly145=
ENST00000534730.5:n.494A>T
ENST00000630659.2:c.*189A>T	ENSP00000486455.1:n.*189A>T
NM_024649.4:c.482A>T	NP_078925.3:p.Glu161Val
NM_024649.5:c.482A>T MANE Select	NP_078925.3:p.Glu161Val