Canonical Allele Identifier: CA2578344481

Gene: AP3B1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78129322del , CM000667.2:g.78129322del	GRCh38
NC_000005.9:g.77425146del , CM000667.1:g.77425146del	GRCh37
NC_000005.8:g.77460902del	NCBI36
NG_007268.1:g.170383del , LRG_170:g.170383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517561.2:c.1651-15del	ENSP00000511839.1:n.1651-15del
ENST00000517940.2:c.1651-15del	ENSP00000511881.1:n.1651-15del
ENST00000519295.6:c.1504-15del	ENSP00000430597.1:n.1504-15del
ENST00000519888.6:c.1651-15del	ENSP00000511880.1:n.1651-15del
ENST00000695447.1:c.1651-15del	ENSP00000511917.1:n.1651-15del
ENST00000695450.1:c.1168-13088del	ENSP00000511919.1:n.1168-13088del
ENST00000695451.1:c.*1417-15del	ENSP00000511920.1:n.*1417-15del
ENST00000695453.1:c.1594-15del	ENSP00000511921.1:n.1594-15del
ENST00000695454.1:c.1645-15del	ENSP00000511922.1:n.1645-15del
ENST00000695455.1:c.1504-15del	ENSP00000511923.1:n.1504-15del
ENST00000695488.1:c.1651-15del	ENSP00000511959.1:n.1651-15del
ENST00000695505.1:n.1809-15del
ENST00000695507.1:c.1651-15del	ENSP00000511970.1:n.1651-15del
ENST00000695510.1:c.1651-15del	ENSP00000511973.1:n.1651-15del
ENST00000695511.1:c.1651-15del	ENSP00000511974.1:n.1651-15del
ENST00000695512.1:c.1651-15del	ENSP00000511975.1:n.1651-15del
ENST00000695513.1:c.1516-15del	ENSP00000511976.1:n.1516-15del
ENST00000695514.1:c.1651-15del	ENSP00000511977.1:n.1651-15del
ENST00000695515.1:c.1651-15del	ENSP00000511978.1:n.1651-15del
ENST00000255194.11:c.1651-15del MANE Select	ENSP00000255194.7:n.1651-15del
ENST00000255194.10:c.1651-15del	ENSP00000255194.6:n.1651-15del
ENST00000517561.1:n.29-15del
ENST00000519295.5:c.1504-15del	ENSP00000430597.1:n.1504-15del
NM_001271769.1:c.1504-15del	NP_001258698.1:n.1504-15del
NM_003664.4:c.1651-15del , LRG_170t1:c.1651-15del	NP_003655.3:n.1651-15del
XM_005248618.2:c.1651-15del	XP_005248675.1:n.1651-15del
XM_005248619.3:c.1651-15del	XP_005248676.1:n.1651-15del
XM_005248618.4:c.1651-15del	XP_005248675.1:n.1651-15del
XM_005248619.5:c.1651-15del	XP_005248676.1:n.1651-15del
XM_017010001.1:c.1504-15del	XP_016865490.1:n.1504-15del
NM_001271769.2:c.1504-15del	NP_001258698.1:n.1504-15del
NM_003664.5:c.1651-15del MANE Select	NP_003655.3:n.1651-15del