Canonical Allele Identifier: CA475368254

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66278142G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66510671G>T , CM000673.2:g.66510671G>T	GRCh38
NC_000011.9:g.66278142G>T , CM000673.1:g.66278142G>T	GRCh37
NC_000011.8:g.66034718G>T	NCBI36
NG_009093.1:g.5024G>T
NG_032068.1:g.35263G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.12G>T MANE Select	ENSP00000317469.7:p.Ala4=
ENST00000318312.11:c.12G>T	ENSP00000317469.7:p.Ala4=
ENST00000393994.4:c.12G>T	ENSP00000377563.2:p.Ala4=
ENST00000419755.3:c.159-342G>T	ENSP00000398526.3:n.159-342G>T
ENST00000455748.6:c.12G>T	ENSP00000405764.2:p.Ala4=
ENST00000524907.5:n.2G>T
ENST00000525809.5:c.12G>T	ENSP00000431187.1:p.Ala4=
ENST00000526035.5:c.12G>T	ENSP00000434197.1:p.Ala4=
ENST00000526760.5:c.12G>T	ENSP00000432140.1:p.Ala4=
ENST00000526815.5:c.-385G>T	ENSP00000436860.1:n.-385G>T
ENST00000527251.5:c.-385G>T	ENSP00000434360.1:n.-385G>T
ENST00000529766.5:n.19G>T
ENST00000529955.5:n.30G>T
ENST00000532908.5:c.12G>T	ENSP00000431866.1:p.Ala4=
ENST00000533557.5:c.12G>T	ENSP00000434619.1:p.Ala4=
ENST00000533644.5:c.12G>T	ENSP00000436073.1:p.Ala4=
ENST00000534730.5:n.24G>T
ENST00000630659.2:c.12G>T	ENSP00000486455.1:p.Ala4=
NM_024649.4:c.12G>T	NP_078925.3:p.Ala4=
NM_024649.5:c.12G>T MANE Select	NP_078925.3:p.Ala4=