Canonical Allele Identifier: CA393301602

Gene: AP3B2 CPEB1-AS1

Linked Data

• dbSNP Id: rs1363557246
• gnomAD v2: 15-83357916-G-C
• gnomAD v4: 15-82689164-G-C
• MyVariant Identifiers: chr15:g.83357916G>C (hg19) ; chr15:g.82689164G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.82689164G>C , CM000677.2:g.82689164G>C	GRCh38
NC_000015.9:g.83357916G>C , CM000677.1:g.83357916G>C	GRCh37
NC_000015.8:g.81154970G>C	NCBI36
NG_052957.1:g.25745C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261722.8:c.258C>G (AP3B2)	ENSP00000261722.4:p.Asn86Lys
ENST00000535359.6:c.258C>G (AP3B2) MANE Select	ENSP00000440984.1:p.Asn86Lys
ENST00000535385.6:n.435C>G (AP3B2)
ENST00000535513.2:c.258C>G (AP3B2)	ENSP00000499258.1:p.Asn86Lys
ENST00000537735.2:n.404C>G (AP3B2)
ENST00000543938.6:n.461C>G (AP3B2)
ENST00000642989.2:c.387C>G (AP3B2)	ENSP00000493485.1:p.Asn129Lys
ENST00000652847.1:c.258C>G (AP3B2)	ENSP00000499785.1:p.Asn86Lys
ENST00000657321.1:c.258C>G (AP3B2)	ENSP00000499716.1:p.Asn86Lys
ENST00000663651.1:n.400C>G (AP3B2)
ENST00000664460.1:c.258C>G (AP3B2)	ENSP00000499798.1:p.Asn86Lys
ENST00000666055.1:c.258C>G (AP3B2)	ENSP00000499608.1:p.Asn86Lys
ENST00000666973.1:c.258C>G (AP3B2)	ENSP00000499288.1:p.Asn86Lys
ENST00000667758.1:c.258C>G (AP3B2)	ENSP00000499318.1:p.Asn86Lys
ENST00000668385.1:c.190-52C>G (AP3B2)	ENSP00000499544.1:n.190-52C>G
ENST00000668990.2:c.258C>G (AP3B2)	ENSP00000499235.1:p.Asn86Lys
ENST00000669930.1:c.189+214C>G (AP3B2)	ENSP00000499671.1:n.189+214C>G
ENST00000679388.1:n.197C>G (AP3B2)
ENST00000679531.1:n.664C>G (AP3B2)
ENST00000679950.1:n.467C>G (AP3B2)
ENST00000680492.1:n.664C>G (AP3B2)
ENST00000680946.1:n.664C>G (AP3B2)
ENST00000681044.1:n.664C>G (AP3B2)
ENST00000681327.1:c.258C>G (AP3B2)	ENSP00000505423.1:p.Asn86Lys
ENST00000681452.1:n.664C>G (AP3B2)
ENST00000681464.1:n.664C>G (AP3B2)
ENST00000261722.7:c.258C>G (AP3B2)	ENSP00000261722.3:p.Asn86Lys
ENST00000535348.5:c.258C>G (AP3B2)	ENSP00000438721.1:p.Asn86Lys
ENST00000535359.5:c.258C>G (AP3B2)	ENSP00000440984.1:p.Asn86Lys
ENST00000535385.5:n.435C>G (AP3B2)
ENST00000535513.1:n.425C>G (AP3B2)
ENST00000541693.5:c.126C>G (AP3B2)	ENSP00000441961.1:p.Asn42Lys
ENST00000542200.2:c.258C>G (AP3B2)	ENSP00000440719.1:p.Asn86Lys
ENST00000561455.5:n.225C>G (AP3B2)
ENST00000620652.4:c.258C>G (AP3B2)	ENSP00000479229.1:p.Asn86Lys
NM_001278511.1:c.258C>G (AP3B2)	NP_001265440.1:p.Asn86Lys
NM_001278512.1:c.258C>G (AP3B2)	NP_001265441.1:p.Asn86Lys
NM_004644.4:c.258C>G (AP3B2)	NP_004635.2:p.Asn86Lys
NR_046096.1:n.1329-2847G>C (CPEB1-AS1)
XM_011522097.1:c.258C>G (AP3B2)	XP_011520399.1:p.Asn86Lys
XM_011522098.1:c.258C>G (AP3B2)	XP_011520400.1:p.Asn86Lys
XM_011522099.1:c.258C>G (AP3B2)	XP_011520401.1:p.Asn86Lys
NM_001348440.1:c.258C>G (AP3B2)	NP_001335369.1:p.Asn86Lys
XM_017022640.2:c.258C>G (AP3B2)	XP_016878129.1:p.Asn86Lys
XM_017022641.2:c.258C>G (AP3B2)	XP_016878130.1:p.Asn86Lys
XR_001751404.2:n.424C>G (AP3B2)
NM_001278512.2:c.258C>G (AP3B2) MANE Select	NP_001265441.1:p.Asn86Lys
NM_004644.5:c.258C>G (AP3B2)	NP_004635.2:p.Asn86Lys
NM_001278511.2:c.258C>G (AP3B2)	NP_001265440.1:p.Asn86Lys
NM_001348440.2:c.258C>G (AP3B2)	NP_001335369.1:p.Asn86Lys