Canonical Allele Identifier: CA360188799

Gene: AP3B1

Linked Data

• MyVariant Identifiers: chr5:g.77437005T>C (hg19) ; chr5:g.78141181T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78141181T>C , CM000667.2:g.78141181T>C	GRCh38
NC_000005.9:g.77437005T>C , CM000667.1:g.77437005T>C	GRCh37
NC_000005.8:g.77472761T>C	NCBI36
NG_007268.1:g.158524A>G , LRG_170:g.158524A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000517561.2:c.1612A>G	ENSP00000511839.1:p.Asn538Asp
ENST00000517940.2:c.1612A>G	ENSP00000511881.1:p.Asn538Asp
ENST00000519295.6:c.1465A>G	ENSP00000430597.1:p.Asn489Asp
ENST00000519888.6:c.1612A>G	ENSP00000511880.1:p.Asn538Asp
ENST00000695447.1:c.1612A>G	ENSP00000511917.1:p.Asn538Asp
ENST00000695450.1:c.1168-24947A>G	ENSP00000511919.1:n.1168-24947A>G
ENST00000695451.1:c.*1378A>G	ENSP00000511920.1:n.*1378A>G
ENST00000695453.1:c.1593+19A>G	ENSP00000511921.1:n.1593+19A>G
ENST00000695454.1:c.1606A>G	ENSP00000511922.1:p.Asn536Asp
ENST00000695455.1:c.1465A>G	ENSP00000511923.1:p.Asn489Asp
ENST00000695488.1:c.1612A>G	ENSP00000511959.1:p.Asn538Asp
ENST00000695505.1:n.1770A>G
ENST00000695507.1:c.1612A>G	ENSP00000511970.1:p.Asn538Asp
ENST00000695510.1:c.1612A>G	ENSP00000511973.1:p.Asn538Asp
ENST00000695511.1:c.1612A>G	ENSP00000511974.1:p.Asn538Asp
ENST00000695512.1:c.1612A>G	ENSP00000511975.1:p.Asn538Asp
ENST00000695513.1:c.1477A>G	ENSP00000511976.1:p.Asn493Asp
ENST00000695514.1:c.1612A>G	ENSP00000511977.1:p.Asn538Asp
ENST00000695515.1:c.1612A>G	ENSP00000511978.1:p.Asn538Asp
ENST00000255194.11:c.1612A>G MANE Select	ENSP00000255194.7:p.Asn538Asp
ENST00000255194.10:c.1612A>G	ENSP00000255194.6:p.Asn538Asp
ENST00000519295.5:c.1465A>G	ENSP00000430597.1:p.Asn489Asp
NM_001271769.1:c.1465A>G	NP_001258698.1:p.Asn489Asp
NM_003664.4:c.1612A>G , LRG_170t1:c.1612A>G	NP_003655.3:p.Asn538Asp
XM_005248618.2:c.1612A>G	XP_005248675.1:p.Asn538Asp
XM_005248619.3:c.1612A>G	XP_005248676.1:p.Asn538Asp
XM_005248618.4:c.1612A>G	XP_005248675.1:p.Asn538Asp
XM_005248619.5:c.1612A>G	XP_005248676.1:p.Asn538Asp
XM_017010001.1:c.1465A>G	XP_016865490.1:p.Asn489Asp
NM_001271769.2:c.1465A>G	NP_001258698.1:p.Asn489Asp
NM_003664.5:c.1612A>G MANE Select	NP_003655.3:p.Asn538Asp