Canonical Allele Identifier: CA491125693

Gene: BBS4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72715346A>G , CM000677.2:g.72715346A>G	GRCh38
NC_000015.9:g.73007687A>G , CM000677.1:g.73007687A>G	GRCh37
NC_000015.8:g.70794740A>G	NCBI36
NG_009416.2:g.34162A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268057.9:c.276A>G MANE Select	ENSP00000268057.4:p.Thr92=
ENST00000268057.8:c.276A>G	ENSP00000268057.4:p.Thr92=
ENST00000395205.6:c.-246A>G	ENSP00000378631.3:n.-246A>G
ENST00000561914.5:c.221-1432A>G	ENSP00000457795.1:n.221-1432A>G
ENST00000562084.5:c.*355A>G	ENSP00000454718.1:n.*355A>G
ENST00000563600.5:c.*226A>G	ENSP00000457753.1:n.*226A>G
ENST00000564239.1:n.343A>G
ENST00000565160.5:c.276A>G	ENSP00000455412.1:p.Thr92=
ENST00000566400.5:c.*161A>G	ENSP00000456759.1:n.*161A>G
ENST00000566829.1:c.294A>G	ENSP00000455958.1:p.Thr98=
ENST00000566938.5:c.*161A>G	ENSP00000456463.1:n.*161A>G
ENST00000567279.5:c.*130A>G	ENSP00000456664.1:n.*130A>G
ENST00000569338.5:c.267A>G	ENSP00000456758.1:p.Thr89=
ENST00000569440.5:c.*220A>G	ENSP00000457958.1:n.*220A>G
NM_001252678.1:c.-246A>G	NP_001239607.1:n.-246A>G
NM_033028.4:c.276A>G	NP_149017.2:p.Thr92=
NR_045565.1:n.383A>G
NR_045566.1:n.638A>G
XM_006720625.2:c.276A>G	XP_006720688.1:p.Thr92=
XM_011521848.1:c.-246A>G	XP_011520150.1:n.-246A>G
XM_011521849.1:c.-184-1432A>G	XP_011520151.1:n.-184-1432A>G
XM_011521850.1:c.-189-1432A>G	XP_011520152.1:n.-189-1432A>G
XM_011521851.1:c.-338A>G	XP_011520153.1:n.-338A>G
NM_001320665.1:c.276A>G	NP_001307594.1:p.Thr92=
XM_017022450.1:c.300A>G	XP_016877939.1:p.Thr100=
XM_017022452.1:c.-184-1432A>G	XP_016877941.1:n.-184-1432A>G
XM_017022453.1:c.-189-1432A>G	XP_016877942.1:n.-189-1432A>G
XM_017022454.1:c.-189-1432A>G	XP_016877943.1:n.-189-1432A>G
NM_033028.5:c.276A>G MANE Select	NP_149017.2:p.Thr92=
NM_001252678.2:c.-246A>G	NP_001239607.1:n.-246A>G
NM_001320665.2:c.276A>G	NP_001307594.1:p.Thr92=
NR_045565.2:n.355A>G
NR_045566.2:n.610A>G