Canonical Allele Identifier: CA381455621

Gene: BBS1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514423T>G , CM000673.2:g.66514423T>G	GRCh38
NC_000011.9:g.66281894T>G , CM000673.1:g.66281894T>G	GRCh37
NC_000011.8:g.66038470T>G	NCBI36
NG_009093.1:g.8776T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.177T>G MANE Select	ENSP00000317469.7:p.Leu59=
ENST00000318312.11:c.177T>G	ENSP00000317469.7:p.Leu59=
ENST00000393994.4:c.177T>G	ENSP00000377563.2:p.Leu59=
ENST00000419755.3:c.288T>G	ENSP00000398526.3:p.Leu96=
ENST00000455748.6:c.177T>G	ENSP00000405764.2:p.Leu59=
ENST00000524458.5:c.52T>G	ENSP00000436195.1:p.Trp18Gly
ENST00000524705.2:c.-20-83T>G	ENSP00000436927.1:n.-20-83T>G
ENST00000524907.5:n.167T>G
ENST00000525809.5:c.160-1117T>G	ENSP00000431187.1:n.160-1117T>G
ENST00000526035.5:c.142T>G	ENSP00000434197.1:p.Trp48Gly
ENST00000526760.5:c.142T>G	ENSP00000432140.1:p.Trp48Gly
ENST00000526815.5:c.87T>G	ENSP00000436860.1:p.Leu29=
ENST00000527251.5:c.52T>G	ENSP00000434360.1:p.Trp18Gly
ENST00000529766.5:n.184T>G
ENST00000529955.5:n.195T>G
ENST00000532908.5:c.142T>G	ENSP00000431866.1:p.Trp48Gly
ENST00000533557.5:c.142T>G	ENSP00000434619.1:p.Trp48Gly
ENST00000533644.5:c.177T>G	ENSP00000436073.1:p.Leu59=
ENST00000534730.5:n.189T>G
ENST00000630659.2:c.142T>G	ENSP00000486455.1:p.Trp48Gly
NM_024649.4:c.177T>G	NP_078925.3:p.Leu59=
NM_024649.5:c.177T>G MANE Select	NP_078925.3:p.Leu59=