Canonical Allele Identifier: CA381455624

Gene: BBS1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66514424G>A , CM000673.2:g.66514424G>A	GRCh38
NC_000011.9:g.66281895G>A , CM000673.1:g.66281895G>A	GRCh37
NC_000011.8:g.66038471G>A	NCBI36
NG_009093.1:g.8777G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318312.12:c.178G>A MANE Select	ENSP00000317469.7:p.Gly60Ser
ENST00000318312.11:c.178G>A	ENSP00000317469.7:p.Gly60Ser
ENST00000393994.4:c.178G>A	ENSP00000377563.2:p.Gly60Ser
ENST00000419755.3:c.289G>A	ENSP00000398526.3:p.Gly97Ser
ENST00000455748.6:c.178G>A	ENSP00000405764.2:p.Gly60Ser
ENST00000524458.5:c.53G>A	ENSP00000436195.1:p.Trp18Ter
ENST00000524705.2:c.-20-82G>A	ENSP00000436927.1:n.-20-82G>A
ENST00000524907.5:n.168G>A
ENST00000525809.5:c.160-1116G>A	ENSP00000431187.1:n.160-1116G>A
ENST00000526035.5:c.143G>A	ENSP00000434197.1:p.Trp48Ter
ENST00000526760.5:c.143G>A	ENSP00000432140.1:p.Trp48Ter
ENST00000526815.5:c.88G>A	ENSP00000436860.1:p.Gly30Ser
ENST00000527251.5:c.53G>A	ENSP00000434360.1:p.Trp18Ter
ENST00000529766.5:n.185G>A
ENST00000529955.5:n.196G>A
ENST00000532908.5:c.143G>A	ENSP00000431866.1:p.Trp48Ter
ENST00000533557.5:c.143G>A	ENSP00000434619.1:p.Trp48Ter
ENST00000533644.5:c.178G>A	ENSP00000436073.1:p.Gly60Ser
ENST00000534730.5:n.190G>A
ENST00000630659.2:c.143G>A	ENSP00000486455.1:p.Trp48Ter
NM_024649.4:c.178G>A	NP_078925.3:p.Gly60Ser
NM_024649.5:c.178G>A MANE Select	NP_078925.3:p.Gly60Ser