Canonical Allele Identifier: CA7699776

Gene: AP3B2 CPEB1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82662255G>T , CM000677.2:g.82662255G>T	GRCh38
NC_000015.9:g.83331007G>T , CM000677.1:g.83331007G>T	GRCh37
NC_000015.8:g.81128062G>T	NCBI36
NG_052957.1:g.52654C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001278512.2:c.2834-3C>A (AP3B2) MANE Select	NP_001265441.1:n.2834-3C>A
ENST00000535359.6:c.2834-3C>A (AP3B2) MANE Select	ENSP00000440984.1:n.2834-3C>A
NM_001278511.1:c.2681-3C>A (AP3B2)	NP_001265440.1:n.2681-3C>A
NM_001278511.2:c.2681-3C>A (AP3B2)	NP_001265440.1:n.2681-3C>A
NM_001278512.1:c.2834-3C>A (AP3B2)	NP_001265441.1:n.2834-3C>A
NM_001348441.1:c.-38C>A (AP3B2)	NP_001335370.1:n.-38C>A
NM_004644.4:c.2777-3C>A (AP3B2)	NP_004635.2:n.2777-3C>A
NM_004644.5:c.2777-3C>A (AP3B2)	NP_004635.2:n.2777-3C>A
NR_046096.1:n.1328+12109G>T (CPEB1-AS1)
ENST00000261722.7:c.2777-3C>A (AP3B2)	ENSP00000261722.3:n.2777-3C>A
ENST00000261722.8:c.2795-3C>A (AP3B2)	ENSP00000261722.4:n.2795-3C>A
ENST00000535348.5:c.2681-3C>A (AP3B2)	ENSP00000438721.1:n.2681-3C>A
ENST00000535359.5:c.2834-3C>A (AP3B2)	ENSP00000440984.1:n.2834-3C>A
ENST00000535385.6:n.3718C>A (AP3B2)
ENST00000537735.1:n.442C>A (AP3B2)
ENST00000537735.2:n.2923-3C>A (AP3B2)
ENST00000543938.5:n.1900-3C>A (AP3B2)
ENST00000543938.6:n.3418C>A (AP3B2)
ENST00000620652.4:c.2777-3C>A (AP3B2)	ENSP00000479229.1:n.2777-3C>A
ENST00000642989.2:c.2906-3C>A (AP3B2)	ENSP00000493485.1:n.2906-3C>A
ENST00000652847.1:c.2777-3C>A (AP3B2)	ENSP00000499785.1:n.2777-3C>A
ENST00000657321.1:c.*2623-3C>A (AP3B2)	ENSP00000499716.1:n.*2623-3C>A
ENST00000660624.1:c.1685-3C>A (AP3B2)	ENSP00000499379.1:n.1685-3C>A
ENST00000661532.1:c.2066-3C>A (AP3B2)
ENST00000663651.1:n.2919-3C>A (AP3B2)
ENST00000666973.1:c.2777-3C>A (AP3B2)	ENSP00000499288.1:n.2777-3C>A
ENST00000667758.1:c.*3429C>A (AP3B2)	ENSP00000499318.1:n.*3429C>A
ENST00000668385.1:c.*2575-3C>A (AP3B2)	ENSP00000499544.1:n.*2575-3C>A
ENST00000668458.1:c.2525-3C>A (AP3B2)
ENST00000668990.2:c.2777-3C>A (AP3B2)	ENSP00000499235.1:n.2777-3C>A
ENST00000669930.1:c.2606-3C>A (AP3B2)	ENSP00000499671.1:n.2606-3C>A
ENST00000679388.1:n.3358C>A (AP3B2)
ENST00000679531.1:n.3621C>A (AP3B2)
ENST00000679891.1:n.1652C>A (AP3B2)
ENST00000679950.1:n.3920C>A (AP3B2)
ENST00000680492.1:n.4254C>A (AP3B2)
ENST00000680912.1:n.2191C>A (AP3B2)
ENST00000680946.1:n.3825C>A (AP3B2)
ENST00000681044.1:n.4331C>A (AP3B2)
ENST00000681327.1:c.*2623-3C>A (AP3B2)	ENSP00000505423.1:n.*2623-3C>A
ENST00000681452.1:n.3183-3C>A (AP3B2)
ENST00000681464.1:n.4127C>A (AP3B2)
XM_011522097.1:c.2762-3C>A (AP3B2)	XP_011520399.1:n.2762-3C>A
XM_011522098.1:c.2738-3C>A (AP3B2)	XP_011520400.1:n.2738-3C>A
XM_011522100.1:c.1685-3C>A (AP3B2)	XP_011520402.1:n.1685-3C>A
XM_017022640.2:c.2705-3C>A (AP3B2)	XP_016878129.1:n.2705-3C>A
XM_024450081.1:c.116-3C>A (AP3B2)	XP_024305849.1:n.116-3C>A
XM_024450082.1:c.-38C>A (AP3B2)	XP_024305850.1:n.-38C>A
XR_001751404.2:n.3005-3C>A (AP3B2)