Canonical Allele Identifier: CA2191485161

Gene: AP3B2 CPEB1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82689158C= , CM000677.2:g.82689158C=	GRCh38
NC_000015.9:g.83357910C= , CM000677.1:g.83357910C=	GRCh37
NC_000015.8:g.81154964C=	NCBI36
NG_052957.1:g.25751G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261722.8:c.264G= (AP3B2)	ENSP00000261722.4:p.Glu88=
ENST00000535359.6:c.264G= (AP3B2) MANE Select	ENSP00000440984.1:p.Glu88=
ENST00000535385.6:n.441G= (AP3B2)
ENST00000535513.2:c.264G= (AP3B2)	ENSP00000499258.1:p.Glu88=
ENST00000537735.2:n.410G= (AP3B2)
ENST00000543938.6:n.467G= (AP3B2)
ENST00000642989.2:c.393G= (AP3B2)	ENSP00000493485.1:p.Glu131=
ENST00000652847.1:c.264G= (AP3B2)	ENSP00000499785.1:p.Glu88=
ENST00000657321.1:c.264G= (AP3B2)	ENSP00000499716.1:p.Glu88=
ENST00000663651.1:n.406G= (AP3B2)
ENST00000664460.1:c.264G= (AP3B2)	ENSP00000499798.1:p.Glu88=
ENST00000666055.1:c.264G= (AP3B2)	ENSP00000499608.1:p.Glu88=
ENST00000666973.1:c.264G= (AP3B2)	ENSP00000499288.1:p.Glu88=
ENST00000667758.1:c.264G= (AP3B2)	ENSP00000499318.1:p.Glu88=
ENST00000668385.1:c.190-46G= (AP3B2)	ENSP00000499544.1:n.190-46G=
ENST00000668990.2:c.264G= (AP3B2)	ENSP00000499235.1:p.Glu88=
ENST00000669930.1:c.189+220G= (AP3B2)	ENSP00000499671.1:n.189+220G=
ENST00000679388.1:n.203G= (AP3B2)
ENST00000679531.1:n.670G= (AP3B2)
ENST00000679950.1:n.473G= (AP3B2)
ENST00000680492.1:n.670G= (AP3B2)
ENST00000680946.1:n.670G= (AP3B2)
ENST00000681044.1:n.670G= (AP3B2)
ENST00000681327.1:c.264G= (AP3B2)	ENSP00000505423.1:p.Glu88=
ENST00000681452.1:n.670G= (AP3B2)
ENST00000681464.1:n.670G= (AP3B2)
ENST00000261722.7:c.264G= (AP3B2)	ENSP00000261722.3:p.Glu88=
ENST00000535348.5:c.264G= (AP3B2)	ENSP00000438721.1:p.Glu88=
ENST00000535359.5:c.264G= (AP3B2)	ENSP00000440984.1:p.Glu88=
ENST00000535385.5:n.441G= (AP3B2)
ENST00000535513.1:n.431G= (AP3B2)
ENST00000541693.5:c.132G= (AP3B2)	ENSP00000441961.1:p.Glu44=
ENST00000542200.2:c.264G= (AP3B2)	ENSP00000440719.1:p.Glu88=
ENST00000561455.5:n.231G= (AP3B2)
ENST00000620652.4:c.264G= (AP3B2)	ENSP00000479229.1:p.Glu88=
NM_001278511.1:c.264G= (AP3B2)	NP_001265440.1:p.Glu88=
NM_001278512.1:c.264G= (AP3B2)	NP_001265441.1:p.Glu88=
NM_004644.4:c.264G= (AP3B2)	NP_004635.2:p.Glu88=
NR_046096.1:n.1329-2853C= (CPEB1-AS1)
XM_011522097.1:c.264G= (AP3B2)	XP_011520399.1:p.Glu88=
XM_011522098.1:c.264G= (AP3B2)	XP_011520400.1:p.Glu88=
XM_011522099.1:c.264G= (AP3B2)	XP_011520401.1:p.Glu88=
NM_001348440.1:c.264G= (AP3B2)	NP_001335369.1:p.Glu88=
XM_017022640.2:c.264G= (AP3B2)	XP_016878129.1:p.Glu88=
XM_017022641.2:c.264G= (AP3B2)	XP_016878130.1:p.Glu88=
XR_001751404.2:n.430G= (AP3B2)
NM_001278512.2:c.264G= (AP3B2) MANE Select	NP_001265441.1:p.Glu88=
NM_004644.5:c.264G= (AP3B2)	NP_004635.2:p.Glu88=
NM_001278511.2:c.264G= (AP3B2)	NP_001265440.1:p.Glu88=
NM_001348440.2:c.264G= (AP3B2)	NP_001335369.1:p.Glu88=