Canonical Allele Identifier: CA7699745
Gene: AP3B2 HGNC NCBI
CPEB1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.82661901G>A , CM000677.2:g.82661901G>A GRCh38
NC_000015.9:g.83330653G>A , CM000677.1:g.83330653G>A GRCh37
NC_000015.8:g.81127708G>A NCBI36
NG_052957.1:g.53008C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001278512.2:c.2940C>T (AP3B2) MANE Select NP_001265441.1:p.Tyr980=
ENST00000535359.6:c.2940C>T (AP3B2) MANE Select ENSP00000440984.1:p.Tyr980=
NM_001278511.1:c.2787C>T (AP3B2) NP_001265440.1:p.Tyr929=
NM_001278511.2:c.2787C>T (AP3B2) NP_001265440.1:p.Tyr929=
NM_001278512.1:c.2940C>T (AP3B2) NP_001265441.1:p.Tyr980=
NM_001348441.1:c.72C>T (AP3B2) NP_001335370.1:p.Tyr24=
NM_001348441.2:c.72C>T (AP3B2) NP_001335370.1:p.Tyr24=
NM_004644.4:c.2883C>T (AP3B2) NP_004635.2:p.Tyr961=
NM_004644.5:c.2883C>T (AP3B2) NP_004635.2:p.Tyr961=
NR_046096.1:n.1328+11755G>A (CPEB1-AS1)
ENST00000261722.7:c.2883C>T (AP3B2) ENSP00000261722.3:p.Tyr961=
ENST00000261722.8:c.2901C>T (AP3B2) ENSP00000261722.4:p.Tyr967=
ENST00000535348.5:c.2787C>T (AP3B2) ENSP00000438721.1:p.Tyr929=
ENST00000535359.5:c.2940C>T (AP3B2) ENSP00000440984.1:p.Tyr980=
ENST00000535385.6:n.3827C>T (AP3B2)
ENST00000537735.1:n.551C>T (AP3B2)
ENST00000537735.2:n.3029C>T (AP3B2)
ENST00000543938.5:n.2006C>T (AP3B2)
ENST00000543938.6:n.3527C>T (AP3B2)
ENST00000620652.4:c.2883C>T (AP3B2) ENSP00000479229.1:p.Tyr961=
ENST00000642989.2:c.3012C>T (AP3B2) ENSP00000493485.1:p.Tyr1004=
ENST00000652847.1:c.2883C>T (AP3B2) ENSP00000499785.1:p.Tyr961=
ENST00000657321.1:c.*2729C>T (AP3B2) ENSP00000499716.1:n.*2729C>T
ENST00000660624.1:c.1791C>T (AP3B2) ENSP00000499379.1:p.Tyr597=
ENST00000661532.1:c.2172C>T (AP3B2)
ENST00000663651.1:n.3025C>T (AP3B2)
ENST00000666973.1:c.2883C>T (AP3B2) ENSP00000499288.1:p.Tyr961=
ENST00000667758.1:c.*3538C>T (AP3B2) ENSP00000499318.1:n.*3538C>T
ENST00000668385.1:c.*2681C>T (AP3B2) ENSP00000499544.1:n.*2681C>T
ENST00000668458.1:c.2631C>T (AP3B2)
ENST00000668990.2:c.2883C>T (AP3B2) ENSP00000499235.1:p.Tyr961=
ENST00000669930.1:c.2712C>T (AP3B2) ENSP00000499671.1:p.Tyr904=
ENST00000679388.1:n.3467C>T (AP3B2)
ENST00000679531.1:n.3730C>T (AP3B2)
ENST00000679891.1:n.1761C>T (AP3B2)
ENST00000679950.1:n.4029C>T (AP3B2)
ENST00000680492.1:n.4363C>T (AP3B2)
ENST00000680912.1:n.2300C>T (AP3B2)
ENST00000680946.1:n.3934C>T (AP3B2)
ENST00000681044.1:n.4440C>T (AP3B2)
ENST00000681327.1:c.*2729C>T (AP3B2) ENSP00000505423.1:n.*2729C>T
ENST00000681452.1:n.3289C>T (AP3B2)
ENST00000681464.1:n.4236C>T (AP3B2)
XM_011522097.1:c.2868C>T (AP3B2) XP_011520399.1:p.Tyr956=
XM_011522098.1:c.2844C>T (AP3B2) XP_011520400.1:p.Tyr948=
XM_011522100.1:c.1791C>T (AP3B2) XP_011520402.1:p.Tyr597=
XM_017022640.2:c.2811C>T (AP3B2) XP_016878129.1:p.Tyr937=
XM_024450081.1:c.222C>T (AP3B2) XP_024305849.1:p.Tyr74=
XM_024450082.1:c.72C>T (AP3B2) XP_024305850.1:p.Tyr24=
XR_001751404.2:n.3111C>T (AP3B2)