Canonical Allele Identifier: CA273479350
Community Standard Title: NM_001278512.2(AP3B2):c.2928C>A (p.Thr976=)
Gene: AP3B2 HGNC NCBI
CPEB1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.82661913G>T , CM000677.2:g.82661913G>T GRCh38
NC_000015.9:g.83330665G>T , CM000677.1:g.83330665G>T GRCh37
NC_000015.8:g.81127720G>T NCBI36
NG_052957.1:g.52996C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001278512.2:c.2928C>A (AP3B2) MANE Select NP_001265441.1:p.Thr976=
ENST00000535359.6:c.2928C>A (AP3B2) MANE Select ENSP00000440984.1:p.Thr976=
NM_001278511.1:c.2775C>A (AP3B2) NP_001265440.1:p.Thr925=
NM_001278511.2:c.2775C>A (AP3B2) NP_001265440.1:p.Thr925=
NM_001278512.1:c.2928C>A (AP3B2) NP_001265441.1:p.Thr976=
NM_001348441.1:c.60C>A (AP3B2) NP_001335370.1:p.Thr20=
NM_001348441.2:c.60C>A (AP3B2) NP_001335370.1:p.Thr20=
NM_004644.4:c.2871C>A (AP3B2) NP_004635.2:p.Thr957=
NM_004644.5:c.2871C>A (AP3B2) NP_004635.2:p.Thr957=
NR_046096.1:n.1328+11767G>T (CPEB1-AS1)
ENST00000261722.7:c.2871C>A (AP3B2) ENSP00000261722.3:p.Thr957=
ENST00000261722.8:c.2889C>A (AP3B2) ENSP00000261722.4:p.Thr963=
ENST00000535348.5:c.2775C>A (AP3B2) ENSP00000438721.1:p.Thr925=
ENST00000535359.5:c.2928C>A (AP3B2) ENSP00000440984.1:p.Thr976=
ENST00000535385.6:n.3815C>A (AP3B2)
ENST00000537735.1:n.539C>A (AP3B2)
ENST00000537735.2:n.3017C>A (AP3B2)
ENST00000543938.5:n.1994C>A (AP3B2)
ENST00000543938.6:n.3515C>A (AP3B2)
ENST00000620652.4:c.2871C>A (AP3B2) ENSP00000479229.1:p.Thr957=
ENST00000642989.2:c.3000C>A (AP3B2) ENSP00000493485.1:p.Thr1000=
ENST00000652847.1:c.2871C>A (AP3B2) ENSP00000499785.1:p.Thr957=
ENST00000657321.1:c.*2717C>A (AP3B2) ENSP00000499716.1:n.*2717C>A
ENST00000660624.1:c.1779C>A (AP3B2) ENSP00000499379.1:p.Thr593=
ENST00000661532.1:c.2160C>A (AP3B2)
ENST00000663651.1:n.3013C>A (AP3B2)
ENST00000666973.1:c.2871C>A (AP3B2) ENSP00000499288.1:p.Thr957=
ENST00000667758.1:c.*3526C>A (AP3B2) ENSP00000499318.1:n.*3526C>A
ENST00000668385.1:c.*2669C>A (AP3B2) ENSP00000499544.1:n.*2669C>A
ENST00000668458.1:c.2619C>A (AP3B2)
ENST00000668990.2:c.2871C>A (AP3B2) ENSP00000499235.1:p.Thr957=
ENST00000669930.1:c.2700C>A (AP3B2) ENSP00000499671.1:p.Thr900=
ENST00000679388.1:n.3455C>A (AP3B2)
ENST00000679531.1:n.3718C>A (AP3B2)
ENST00000679891.1:n.1749C>A (AP3B2)
ENST00000679950.1:n.4017C>A (AP3B2)
ENST00000680492.1:n.4351C>A (AP3B2)
ENST00000680912.1:n.2288C>A (AP3B2)
ENST00000680946.1:n.3922C>A (AP3B2)
ENST00000681044.1:n.4428C>A (AP3B2)
ENST00000681327.1:c.*2717C>A (AP3B2) ENSP00000505423.1:n.*2717C>A
ENST00000681452.1:n.3277C>A (AP3B2)
ENST00000681464.1:n.4224C>A (AP3B2)
XM_011522097.1:c.2856C>A (AP3B2) XP_011520399.1:p.Thr952=
XM_011522098.1:c.2832C>A (AP3B2) XP_011520400.1:p.Thr944=
XM_011522100.1:c.1779C>A (AP3B2) XP_011520402.1:p.Thr593=
XM_017022640.2:c.2799C>A (AP3B2) XP_016878129.1:p.Thr933=
XM_024450081.1:c.210C>A (AP3B2) XP_024305849.1:p.Thr70=
XM_024450082.1:c.60C>A (AP3B2) XP_024305850.1:p.Thr20=
XR_001751404.2:n.3099C>A (AP3B2)