Canonical Allele Identifier: CA381455918

Gene: BBS1

Linked Data

• MyVariant Identifiers: chr11:g.66281930C>G (hg19) ; chr11:g.66514459C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514459C>G , CM000673.2:g.66514459C>G	GRCh38
NC_000011.9:g.66281930C>G , CM000673.1:g.66281930C>G	GRCh37
NC_000011.8:g.66038506C>G	NCBI36
NG_009093.1:g.8812C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.213C>G MANE Select	ENSP00000317469.7:p.Leu71=
ENST00000318312.11:c.213C>G	ENSP00000317469.7:p.Leu71=
ENST00000393994.4:c.213C>G	ENSP00000377563.2:p.Leu71=
ENST00000419755.3:c.324C>G	ENSP00000398526.3:p.Leu108=
ENST00000455748.6:c.213C>G	ENSP00000405764.2:p.Leu71=
ENST00000524458.5:c.88C>G	ENSP00000436195.1:p.Gln30Glu
ENST00000524705.2:c.-20-47C>G	ENSP00000436927.1:n.-20-47C>G
ENST00000524907.5:n.203C>G
ENST00000525809.5:c.160-1081C>G	ENSP00000431187.1:n.160-1081C>G
ENST00000526035.5:c.178C>G	ENSP00000434197.1:p.Gln60Glu
ENST00000526760.5:c.178C>G	ENSP00000432140.1:p.Gln60Glu
ENST00000526815.5:c.123C>G	ENSP00000436860.1:p.Leu41=
ENST00000527251.5:c.88C>G	ENSP00000434360.1:p.Gln30Glu
ENST00000529766.5:n.220C>G
ENST00000529955.5:n.231C>G
ENST00000532908.5:c.178C>G	ENSP00000431866.1:p.Gln60Glu
ENST00000533557.5:c.178C>G	ENSP00000434619.1:p.Gln60Glu
ENST00000533644.5:c.213C>G	ENSP00000436073.1:p.Leu71=
ENST00000534730.5:n.225C>G
ENST00000630659.2:c.178C>G	ENSP00000486455.1:p.Gln60Glu
NM_024649.4:c.213C>G	NP_078925.3:p.Leu71=
NM_024649.5:c.213C>G MANE Select	NP_078925.3:p.Leu71=