Canonical Allele Identifier: CA393301641

Gene: AP3B2 CPEB1-AS1

Linked Data

• gnomAD v4: 15-82689171-C-T
• MyVariant Identifiers: chr15:g.83357923C>T (hg19) ; chr15:g.82689171C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82689171C>T , CM000677.2:g.82689171C>T	GRCh38
NC_000015.9:g.83357923C>T , CM000677.1:g.83357923C>T	GRCh37
NC_000015.8:g.81154977C>T	NCBI36
NG_052957.1:g.25738G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261722.8:c.251G>A (AP3B2)	ENSP00000261722.4:p.Cys84Tyr
ENST00000535359.6:c.251G>A (AP3B2) MANE Select	ENSP00000440984.1:p.Cys84Tyr
ENST00000535385.6:n.428G>A (AP3B2)
ENST00000535513.2:c.251G>A (AP3B2)	ENSP00000499258.1:p.Cys84Tyr
ENST00000537735.2:n.397G>A (AP3B2)
ENST00000543938.6:n.454G>A (AP3B2)
ENST00000642989.2:c.380G>A (AP3B2)	ENSP00000493485.1:p.Cys127Tyr
ENST00000652847.1:c.251G>A (AP3B2)	ENSP00000499785.1:p.Cys84Tyr
ENST00000657321.1:c.251G>A (AP3B2)	ENSP00000499716.1:p.Cys84Tyr
ENST00000663651.1:n.393G>A (AP3B2)
ENST00000664460.1:c.251G>A (AP3B2)	ENSP00000499798.1:p.Cys84Tyr
ENST00000666055.1:c.251G>A (AP3B2)	ENSP00000499608.1:p.Cys84Tyr
ENST00000666973.1:c.251G>A (AP3B2)	ENSP00000499288.1:p.Cys84Tyr
ENST00000667758.1:c.251G>A (AP3B2)	ENSP00000499318.1:p.Cys84Tyr
ENST00000668385.1:c.190-59G>A (AP3B2)	ENSP00000499544.1:n.190-59G>A
ENST00000668990.2:c.251G>A (AP3B2)	ENSP00000499235.1:p.Cys84Tyr
ENST00000669930.1:c.189+207G>A (AP3B2)	ENSP00000499671.1:n.189+207G>A
ENST00000679388.1:n.190G>A (AP3B2)
ENST00000679531.1:n.657G>A (AP3B2)
ENST00000679950.1:n.460G>A (AP3B2)
ENST00000680492.1:n.657G>A (AP3B2)
ENST00000680946.1:n.657G>A (AP3B2)
ENST00000681044.1:n.657G>A (AP3B2)
ENST00000681327.1:c.251G>A (AP3B2)	ENSP00000505423.1:p.Cys84Tyr
ENST00000681452.1:n.657G>A (AP3B2)
ENST00000681464.1:n.657G>A (AP3B2)
ENST00000261722.7:c.251G>A (AP3B2)	ENSP00000261722.3:p.Cys84Tyr
ENST00000535348.5:c.251G>A (AP3B2)	ENSP00000438721.1:p.Cys84Tyr
ENST00000535359.5:c.251G>A (AP3B2)	ENSP00000440984.1:p.Cys84Tyr
ENST00000535385.5:n.428G>A (AP3B2)
ENST00000535513.1:n.418G>A (AP3B2)
ENST00000541693.5:c.119G>A (AP3B2)	ENSP00000441961.1:p.Cys40Tyr
ENST00000542200.2:c.251G>A (AP3B2)	ENSP00000440719.1:p.Cys84Tyr
ENST00000561455.5:n.218G>A (AP3B2)
ENST00000620652.4:c.251G>A (AP3B2)	ENSP00000479229.1:p.Cys84Tyr
NM_001278511.1:c.251G>A (AP3B2)	NP_001265440.1:p.Cys84Tyr
NM_001278512.1:c.251G>A (AP3B2)	NP_001265441.1:p.Cys84Tyr
NM_004644.4:c.251G>A (AP3B2)	NP_004635.2:p.Cys84Tyr
NR_046096.1:n.1329-2840C>T (CPEB1-AS1)
XM_011522097.1:c.251G>A (AP3B2)	XP_011520399.1:p.Cys84Tyr
XM_011522098.1:c.251G>A (AP3B2)	XP_011520400.1:p.Cys84Tyr
XM_011522099.1:c.251G>A (AP3B2)	XP_011520401.1:p.Cys84Tyr
NM_001348440.1:c.251G>A (AP3B2)	NP_001335369.1:p.Cys84Tyr
XM_017022640.2:c.251G>A (AP3B2)	XP_016878129.1:p.Cys84Tyr
XM_017022641.2:c.251G>A (AP3B2)	XP_016878130.1:p.Cys84Tyr
XR_001751404.2:n.417G>A (AP3B2)
NM_001278512.2:c.251G>A (AP3B2) MANE Select	NP_001265441.1:p.Cys84Tyr
NM_004644.5:c.251G>A (AP3B2)	NP_004635.2:p.Cys84Tyr
NM_001278511.2:c.251G>A (AP3B2)	NP_001265440.1:p.Cys84Tyr
NM_001348440.2:c.251G>A (AP3B2)	NP_001335369.1:p.Cys84Tyr