Canonical Allele Identifier: CA7700093

Gene: AP3B2 CPEB1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82665580G>T , CM000677.2:g.82665580G>T	GRCh38
NC_000015.9:g.83334332G>T , CM000677.1:g.83334332G>T	GRCh37
NC_000015.8:g.81131387G>T	NCBI36
NG_052957.1:g.49329C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001278512.2:c.1853-5C>A (AP3B2) MANE Select	NP_001265441.1:n.1853-5C>A
ENST00000535359.6:c.1853-5C>A (AP3B2) MANE Select	ENSP00000440984.1:n.1853-5C>A
NM_001278511.1:c.1757-5C>A (AP3B2)	NP_001265440.1:n.1757-5C>A
NM_001278511.2:c.1757-5C>A (AP3B2)	NP_001265440.1:n.1757-5C>A
NM_001278512.1:c.1853-5C>A (AP3B2)	NP_001265441.1:n.1853-5C>A
NM_004644.4:c.1853-5C>A (AP3B2)	NP_004635.2:n.1853-5C>A
NM_004644.5:c.1853-5C>A (AP3B2)	NP_004635.2:n.1853-5C>A
NR_046096.1:n.1328+15434G>T (CPEB1-AS1)
ENST00000261722.7:c.1853-5C>A (AP3B2)	ENSP00000261722.3:n.1853-5C>A
ENST00000261722.8:c.1853-5C>A (AP3B2)	ENSP00000261722.4:n.1853-5C>A
ENST00000535348.5:c.1757-5C>A (AP3B2)	ENSP00000438721.1:n.1757-5C>A
ENST00000535359.5:c.1853-5C>A (AP3B2)	ENSP00000440984.1:n.1853-5C>A
ENST00000535385.6:n.2356-5C>A (AP3B2)
ENST00000537735.2:n.1999-5C>A (AP3B2)
ENST00000543938.5:n.976-5C>A (AP3B2)
ENST00000543938.6:n.2056-5C>A (AP3B2)
ENST00000620652.4:c.1853-5C>A (AP3B2)	ENSP00000479229.1:n.1853-5C>A
ENST00000642989.2:c.1982-5C>A (AP3B2)	ENSP00000493485.1:n.1982-5C>A
ENST00000652847.1:c.1853-5C>A (AP3B2)	ENSP00000499785.1:n.1853-5C>A
ENST00000657321.1:c.*1602-5C>A (AP3B2)	ENSP00000499716.1:n.*1602-5C>A
ENST00000660624.1:c.761-5C>A (AP3B2)	ENSP00000499379.1:n.761-5C>A
ENST00000661532.1:c.1080-5C>A (AP3B2)
ENST00000663651.1:n.1995-5C>A (AP3B2)
ENST00000666973.1:c.1853-5C>A (AP3B2)	ENSP00000499288.1:n.1853-5C>A
ENST00000667758.1:c.*1741-5C>A (AP3B2)	ENSP00000499318.1:n.*1741-5C>A
ENST00000668385.1:c.*1651-5C>A (AP3B2)	ENSP00000499544.1:n.*1651-5C>A
ENST00000668458.1:c.1474-5C>A (AP3B2)
ENST00000668990.2:c.1853-5C>A (AP3B2)	ENSP00000499235.1:n.1853-5C>A
ENST00000669930.1:c.1682-5C>A (AP3B2)	ENSP00000499671.1:n.1682-5C>A
ENST00000679388.1:n.1792-5C>A (AP3B2)
ENST00000679531.1:n.2259-5C>A (AP3B2)
ENST00000679891.1:n.285C>A (AP3B2)
ENST00000679950.1:n.2232-5C>A (AP3B2)
ENST00000680492.1:n.2259-5C>A (AP3B2)
ENST00000680912.1:n.418C>A (AP3B2)
ENST00000680946.1:n.2259-5C>A (AP3B2)
ENST00000681044.1:n.2259-5C>A (AP3B2)
ENST00000681327.1:c.*1602-5C>A (AP3B2)	ENSP00000505423.1:n.*1602-5C>A
ENST00000681452.1:n.2259-5C>A (AP3B2)
ENST00000681464.1:n.2259-5C>A (AP3B2)
XM_011522097.1:c.1781-5C>A (AP3B2)	XP_011520399.1:n.1781-5C>A
XM_011522098.1:c.1757-5C>A (AP3B2)	XP_011520400.1:n.1757-5C>A
XM_011522099.1:c.1853-5C>A (AP3B2)	XP_011520401.1:n.1853-5C>A
XM_011522100.1:c.761-5C>A (AP3B2)	XP_011520402.1:n.761-5C>A
XM_017022640.2:c.1781-5C>A (AP3B2)	XP_016878129.1:n.1781-5C>A
XR_001751404.2:n.2019-5C>A (AP3B2)