Canonical Allele Identifier: CA7699769
Gene: AP3B2 HGNC NCBI
CPEB1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.82662153G>A , CM000677.2:g.82662153G>A GRCh38
NC_000015.9:g.83330905G>A , CM000677.1:g.83330905G>A GRCh37
NC_000015.8:g.81127960G>A NCBI36
NG_052957.1:g.52756C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001278512.2:c.2918+15C>T (AP3B2) MANE Select NP_001265441.1:n.2918+15C>T
ENST00000535359.6:c.2918+15C>T (AP3B2) MANE Select ENSP00000440984.1:n.2918+15C>T
NM_001278511.1:c.2765+15C>T (AP3B2) NP_001265440.1:n.2765+15C>T
NM_001278511.2:c.2765+15C>T (AP3B2) NP_001265440.1:n.2765+15C>T
NM_001278512.1:c.2918+15C>T (AP3B2) NP_001265441.1:n.2918+15C>T
NM_001348441.1:c.50+15C>T (AP3B2) NP_001335370.1:n.50+15C>T
NM_001348441.2:c.50+15C>T (AP3B2) NP_001335370.1:n.50+15C>T
NM_004644.4:c.2861+15C>T (AP3B2) NP_004635.2:n.2861+15C>T
NM_004644.5:c.2861+15C>T (AP3B2) NP_004635.2:n.2861+15C>T
NR_046096.1:n.1328+12007G>A (CPEB1-AS1)
ENST00000261722.7:c.2861+15C>T (AP3B2) ENSP00000261722.3:n.2861+15C>T
ENST00000261722.8:c.2879+15C>T (AP3B2) ENSP00000261722.4:n.2879+15C>T
ENST00000535348.5:c.2765+15C>T (AP3B2) ENSP00000438721.1:n.2765+15C>T
ENST00000535359.5:c.2918+15C>T (AP3B2) ENSP00000440984.1:n.2918+15C>T
ENST00000535385.6:n.3805+15C>T (AP3B2)
ENST00000537735.1:n.529+15C>T (AP3B2)
ENST00000537735.2:n.3007+15C>T (AP3B2)
ENST00000543938.5:n.1984+15C>T (AP3B2)
ENST00000543938.6:n.3505+15C>T (AP3B2)
ENST00000620652.4:c.2861+15C>T (AP3B2) ENSP00000479229.1:n.2861+15C>T
ENST00000642989.2:c.2990+15C>T (AP3B2) ENSP00000493485.1:n.2990+15C>T
ENST00000652847.1:c.2861+15C>T (AP3B2) ENSP00000499785.1:n.2861+15C>T
ENST00000657321.1:c.*2707+15C>T (AP3B2) ENSP00000499716.1:n.*2707+15C>T
ENST00000660624.1:c.1769+15C>T (AP3B2) ENSP00000499379.1:n.1769+15C>T
ENST00000661532.1:c.2150+15C>T (AP3B2)
ENST00000663651.1:n.3003+15C>T (AP3B2)
ENST00000666973.1:c.2861+15C>T (AP3B2) ENSP00000499288.1:n.2861+15C>T
ENST00000667758.1:c.*3516+15C>T (AP3B2) ENSP00000499318.1:n.*3516+15C>T
ENST00000668385.1:c.*2659+15C>T (AP3B2) ENSP00000499544.1:n.*2659+15C>T
ENST00000668458.1:c.2609+15C>T (AP3B2)
ENST00000668990.2:c.2861+15C>T (AP3B2) ENSP00000499235.1:n.2861+15C>T
ENST00000669930.1:c.2690+15C>T (AP3B2) ENSP00000499671.1:n.2690+15C>T
ENST00000679388.1:n.3445+15C>T (AP3B2)
ENST00000679531.1:n.3708+15C>T (AP3B2)
ENST00000679891.1:n.1739+15C>T (AP3B2)
ENST00000679950.1:n.4007+15C>T (AP3B2)
ENST00000680492.1:n.4341+15C>T (AP3B2)
ENST00000680912.1:n.2278+15C>T (AP3B2)
ENST00000680946.1:n.3912+15C>T (AP3B2)
ENST00000681044.1:n.4418+15C>T (AP3B2)
ENST00000681327.1:c.*2707+15C>T (AP3B2) ENSP00000505423.1:n.*2707+15C>T
ENST00000681452.1:n.3267+15C>T (AP3B2)
ENST00000681464.1:n.4214+15C>T (AP3B2)
XM_011522097.1:c.2846+15C>T (AP3B2) XP_011520399.1:n.2846+15C>T
XM_011522098.1:c.2822+15C>T (AP3B2) XP_011520400.1:n.2822+15C>T
XM_011522100.1:c.1769+15C>T (AP3B2) XP_011520402.1:n.1769+15C>T
XM_017022640.2:c.2789+15C>T (AP3B2) XP_016878129.1:n.2789+15C>T
XM_024450081.1:c.200+15C>T (AP3B2) XP_024305849.1:n.200+15C>T
XM_024450082.1:c.50+15C>T (AP3B2) XP_024305850.1:n.50+15C>T
XR_001751404.2:n.3089+15C>T (AP3B2)