Canonical Allele Identifier: CA381456387

Gene: BBS1

Linked Data

• ClinVar Variation Id: 2836021
• ClinVar RCV Id: RCV003635006
• MyVariant Identifiers: chr11:g.66281993C>T (hg19) ; chr11:g.66514522C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514522C>T , CM000673.2:g.66514522C>T	GRCh38
NC_000011.9:g.66281993C>T , CM000673.1:g.66281993C>T	GRCh37
NC_000011.8:g.66038569C>T	NCBI36
NG_009093.1:g.8875C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.276C>T MANE Select	ENSP00000317469.7:p.Phe92=
ENST00000318312.11:c.276C>T	ENSP00000317469.7:p.Phe92=
ENST00000393994.4:c.276C>T	ENSP00000377563.2:p.Phe92=
ENST00000419755.3:c.387C>T	ENSP00000398526.3:p.Phe129=
ENST00000455748.6:c.276C>T	ENSP00000405764.2:p.Phe92=
ENST00000524458.5:c.151C>T	ENSP00000436195.1:p.Pro51Ser
ENST00000524705.2:c.-4C>T	ENSP00000436927.1:n.-4C>T
ENST00000524907.5:n.266C>T
ENST00000525809.5:c.160-1018C>T	ENSP00000431187.1:n.160-1018C>T
ENST00000526035.5:c.241C>T	ENSP00000434197.1:p.Pro81Ser
ENST00000526760.5:c.241C>T	ENSP00000432140.1:p.Pro81Ser
ENST00000527251.5:c.151C>T	ENSP00000434360.1:p.Pro51Ser
ENST00000529766.5:n.283C>T
ENST00000529955.5:n.294C>T
ENST00000532908.5:c.241C>T	ENSP00000431866.1:p.Pro81Ser
ENST00000533430.5:n.54C>T
ENST00000533557.5:c.241C>T	ENSP00000434619.1:p.Pro81Ser
ENST00000533644.5:c.276C>T	ENSP00000436073.1:p.Phe92=
ENST00000534730.5:n.288C>T
ENST00000630659.2:c.241C>T	ENSP00000486455.1:p.Pro81Ser
NM_024649.4:c.276C>T	NP_078925.3:p.Phe92=
NM_024649.5:c.276C>T MANE Select	NP_078925.3:p.Phe92=