Canonical Allele Identifier: CA2580090087

Gene: AP3B2 CPEB1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82661821_82661822dup , CM000677.2:g.82661821_82661822dup	GRCh38
NC_000015.9:g.83330573_83330574dup , CM000677.1:g.83330573_83330574dup	GRCh37
NC_000015.8:g.81127628_81127629dup	NCBI36
NG_052957.1:g.53088_53089dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001278512.2:c.3016+4_3016+5dup (AP3B2) MANE Select	NP_001265441.1:n.3016+4_3016+5dup
ENST00000535359.6:c.3016+4_3016+5dup (AP3B2) MANE Select	ENSP00000440984.1:n.3016+4_3016+5dup
NM_001278511.1:c.2863+4_2863+5dup (AP3B2)	NP_001265440.1:n.2863+4_2863+5dup
NM_001278511.2:c.2863+4_2863+5dup (AP3B2)	NP_001265440.1:n.2863+4_2863+5dup
NM_001278512.1:c.3016+4_3016+5dup (AP3B2)	NP_001265441.1:n.3016+4_3016+5dup
NM_001348441.1:c.148+4_148+5dup (AP3B2)	NP_001335370.1:n.148+4_148+5dup
NM_001348441.2:c.148+4_148+5dup (AP3B2)	NP_001335370.1:n.148+4_148+5dup
NM_004644.4:c.2959+4_2959+5dup (AP3B2)	NP_004635.2:n.2959+4_2959+5dup
NM_004644.5:c.2959+4_2959+5dup (AP3B2)	NP_004635.2:n.2959+4_2959+5dup
NR_046096.1:n.1328+11675_1328+11676dup (CPEB1-AS1)
ENST00000261722.7:c.2959+4_2959+5dup (AP3B2)	ENSP00000261722.3:n.2959+4_2959+5dup
ENST00000261722.8:c.2977+4_2977+5dup (AP3B2)	ENSP00000261722.4:n.2977+4_2977+5dup
ENST00000535348.5:c.2863+4_2863+5dup (AP3B2)	ENSP00000438721.1:n.2863+4_2863+5dup
ENST00000535359.5:c.3016+4_3016+5dup (AP3B2)	ENSP00000440984.1:n.3016+4_3016+5dup
ENST00000535385.6:n.3903+4_3903+5dup (AP3B2)
ENST00000537735.1:n.627+4_627+5dup (AP3B2)
ENST00000537735.2:n.3105+4_3105+5dup (AP3B2)
ENST00000543938.5:n.2082+4_2082+5dup (AP3B2)
ENST00000543938.6:n.3603+4_3603+5dup (AP3B2)
ENST00000620652.4:c.2959+4_2959+5dup (AP3B2)	ENSP00000479229.1:n.2959+4_2959+5dup
ENST00000642989.2:c.3088+4_3088+5dup (AP3B2)	ENSP00000493485.1:n.3088+4_3088+5dup
ENST00000652847.1:c.2959+4_2959+5dup (AP3B2)	ENSP00000499785.1:n.2959+4_2959+5dup
ENST00000657321.1:c.*2805+4_*2805+5dup (AP3B2)	ENSP00000499716.1:n.*2805+4_*2805+5dup
ENST00000660624.1:c.1867+4_1867+5dup (AP3B2)	ENSP00000499379.1:n.1867+4_1867+5dup
ENST00000661532.1:c.2248+4_2248+5dup (AP3B2)
ENST00000663651.1:n.3101+4_3101+5dup (AP3B2)
ENST00000666973.1:c.2959+4_2959+5dup (AP3B2)	ENSP00000499288.1:n.2959+4_2959+5dup
ENST00000667758.1:c.*3614+4_*3614+5dup (AP3B2)	ENSP00000499318.1:n.*3614+4_*3614+5dup
ENST00000668385.1:c.*2757+4_*2757+5dup (AP3B2)	ENSP00000499544.1:n.*2757+4_*2757+5dup
ENST00000668458.1:c.2707+4_2707+5dup (AP3B2)
ENST00000668990.2:c.2959+4_2959+5dup (AP3B2)	ENSP00000499235.1:n.2959+4_2959+5dup
ENST00000669930.1:c.2788+4_2788+5dup (AP3B2)	ENSP00000499671.1:n.2788+4_2788+5dup
ENST00000679388.1:n.3543+4_3543+5dup (AP3B2)
ENST00000679531.1:n.3810_3811dup (AP3B2)
ENST00000679891.1:n.1837+4_1837+5dup (AP3B2)
ENST00000679950.1:n.4105+4_4105+5dup (AP3B2)
ENST00000680492.1:n.4439+4_4439+5dup (AP3B2)
ENST00000680912.1:n.2376+4_2376+5dup (AP3B2)
ENST00000680946.1:n.4010+4_4010+5dup (AP3B2)
ENST00000681044.1:n.4516+4_4516+5dup (AP3B2)
ENST00000681327.1:c.*2805+4_*2805+5dup (AP3B2)	ENSP00000505423.1:n.*2805+4_*2805+5dup
ENST00000681452.1:n.3369_3370dup (AP3B2)
ENST00000681464.1:n.4312+4_4312+5dup (AP3B2)
XM_011522097.1:c.2944+4_2944+5dup (AP3B2)	XP_011520399.1:n.2944+4_2944+5dup
XM_011522098.1:c.2920+4_2920+5dup (AP3B2)	XP_011520400.1:n.2920+4_2920+5dup
XM_011522100.1:c.1867+4_1867+5dup (AP3B2)	XP_011520402.1:n.1867+4_1867+5dup
XM_017022640.2:c.2887+4_2887+5dup (AP3B2)	XP_016878129.1:n.2887+4_2887+5dup
XM_024450081.1:c.298+4_298+5dup (AP3B2)	XP_024305849.1:n.298+4_298+5dup
XM_024450082.1:c.148+4_148+5dup (AP3B2)	XP_024305850.1:n.148+4_148+5dup
XR_001751404.2:n.3187+4_3187+5dup (AP3B2)