Canonical Allele Identifier: CA393309496

Gene: AP3B2 CPEB1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.83331908T>A (hg19) ; chr15:g.82663156T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82663156T>A , CM000677.2:g.82663156T>A	GRCh38
NC_000015.9:g.83331908T>A , CM000677.1:g.83331908T>A	GRCh37
NC_000015.8:g.81128963T>A	NCBI36
NG_052957.1:g.51753A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261722.8:c.2536A>T (AP3B2)	ENSP00000261722.4:p.Thr846Ser
ENST00000535359.6:c.2575A>T (AP3B2) MANE Select	ENSP00000440984.1:p.Thr859Ser
ENST00000535385.6:n.3021A>T (AP3B2)
ENST00000537735.2:n.2664A>T (AP3B2)
ENST00000543938.6:n.2721A>T (AP3B2)
ENST00000642989.2:c.2647A>T (AP3B2)	ENSP00000493485.1:p.Thr883Ser
ENST00000652847.1:c.2518A>T (AP3B2)	ENSP00000499785.1:p.Thr840Ser
ENST00000657321.1:c.*2593A>T (AP3B2)	ENSP00000499716.1:n.*2593A>T
ENST00000660624.1:c.1426A>T (AP3B2)	ENSP00000499379.1:p.Thr476Ser
ENST00000661532.1:c.1807A>T (AP3B2)
ENST00000663651.1:n.2660A>T (AP3B2)
ENST00000666973.1:c.2518A>T (AP3B2)	ENSP00000499288.1:p.Thr840Ser
ENST00000667758.1:c.*2732A>T (AP3B2)	ENSP00000499318.1:n.*2732A>T
ENST00000668385.1:c.*2316A>T (AP3B2)	ENSP00000499544.1:n.*2316A>T
ENST00000668458.1:c.2266A>T (AP3B2)
ENST00000668990.2:c.2518A>T (AP3B2)	ENSP00000499235.1:p.Thr840Ser
ENST00000669930.1:c.2347A>T (AP3B2)	ENSP00000499671.1:p.Thr783Ser
ENST00000679388.1:n.2457A>T (AP3B2)
ENST00000679531.1:n.2924A>T (AP3B2)
ENST00000679891.1:n.955A>T (AP3B2)
ENST00000679950.1:n.3223A>T (AP3B2)
ENST00000680492.1:n.3557A>T (AP3B2)
ENST00000680912.1:n.1494A>T (AP3B2)
ENST00000680946.1:n.2924A>T (AP3B2)
ENST00000681044.1:n.3430A>T (AP3B2)
ENST00000681327.1:c.*2593A>T (AP3B2)	ENSP00000505423.1:n.*2593A>T
ENST00000681452.1:n.2924A>T (AP3B2)
ENST00000681464.1:n.3430A>T (AP3B2)
ENST00000261722.7:c.2518A>T (AP3B2)	ENSP00000261722.3:p.Thr840Ser
ENST00000535348.5:c.2422A>T (AP3B2)	ENSP00000438721.1:p.Thr808Ser
ENST00000535359.5:c.2575A>T (AP3B2)	ENSP00000440984.1:p.Thr859Ser
ENST00000538592.1:c.165A>T (AP3B2)	ENSP00000445804.1:n.165A>T
ENST00000543938.5:n.1641A>T (AP3B2)
ENST00000545315.1:n.94A>T (AP3B2)
ENST00000620652.4:c.2518A>T (AP3B2)	ENSP00000479229.1:p.Thr840Ser
NM_001278511.1:c.2422A>T (AP3B2)	NP_001265440.1:p.Thr808Ser
NM_001278512.1:c.2575A>T (AP3B2)	NP_001265441.1:p.Thr859Ser
NM_004644.4:c.2518A>T (AP3B2)	NP_004635.2:p.Thr840Ser
NR_046096.1:n.1328+13010T>A (CPEB1-AS1)
XM_011522097.1:c.2503A>T (AP3B2)	XP_011520399.1:p.Thr835Ser
XM_011522098.1:c.2479A>T (AP3B2)	XP_011520400.1:p.Thr827Ser
XM_011522100.1:c.1426A>T (AP3B2)	XP_011520402.1:p.Thr476Ser
XM_017022640.2:c.2446A>T (AP3B2)	XP_016878129.1:p.Thr816Ser
XM_024450081.1:c.-144A>T (AP3B2)	XP_024305849.1:n.-144A>T
XM_024450082.1:c.-735A>T (AP3B2)	XP_024305850.1:n.-735A>T
XR_001751404.2:n.2746A>T (AP3B2)
NM_001278512.2:c.2575A>T (AP3B2) MANE Select	NP_001265441.1:p.Thr859Ser
NM_004644.5:c.2518A>T (AP3B2)	NP_004635.2:p.Thr840Ser
NM_001278511.2:c.2422A>T (AP3B2)	NP_001265440.1:p.Thr808Ser