Canonical Allele Identifier: CA1557269234

Gene: AP3B1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78039140T= , CM000667.2:g.78039140T=	GRCh38
NC_000005.9:g.77334964T= , CM000667.1:g.77334964T=	GRCh37
NC_000005.8:g.77370720T=	NCBI36
NG_007268.1:g.260565A= , LRG_170:g.260565A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519295.6:c.2565A=	ENSP00000430597.1:p.Ile855=
ENST00000523204.2:n.512A=
ENST00000695447.1:c.2605A=	ENSP00000511917.1:n.2605A=
ENST00000695450.1:c.1911A=	ENSP00000511919.1:p.Ile637=
ENST00000695451.1:c.*2474A=	ENSP00000511920.1:n.*2474A=
ENST00000695453.1:c.2655A=	ENSP00000511921.1:p.Ile885=
ENST00000695454.1:c.2706A=	ENSP00000511922.1:p.Ile902=
ENST00000695455.1:c.2565A=	ENSP00000511923.1:p.Ile855=
ENST00000695458.1:n.427A=
ENST00000695488.1:c.2712A=	ENSP00000511959.1:p.Ile904=
ENST00000695505.1:n.2870A=
ENST00000695506.1:n.364A=
ENST00000695507.1:c.*237A=	ENSP00000511970.1:n.*237A=
ENST00000695510.1:c.2712A=	ENSP00000511973.1:p.Ile904=
ENST00000695511.1:c.2712A=	ENSP00000511974.1:p.Ile904=
ENST00000695512.1:c.2532A=	ENSP00000511975.1:p.Ile844=
ENST00000695513.1:c.2577A=	ENSP00000511976.1:p.Ile859=
ENST00000695515.1:c.2712A=	ENSP00000511978.1:p.Ile904=
ENST00000255194.11:c.2712A= MANE Select	ENSP00000255194.7:p.Ile904=
ENST00000255194.10:c.2712A=	ENSP00000255194.6:p.Ile904=
ENST00000519295.5:c.2565A=	ENSP00000430597.1:p.Ile855=
ENST00000522901.1:c.11A=
ENST00000523204.1:n.512A=
NM_001271769.1:c.2565A=	NP_001258698.1:p.Ile855=
NM_003664.4:c.2712A= , LRG_170t1:c.2712A=	NP_003655.3:p.Ile904=
XM_005248618.2:c.2712A=	XP_005248675.1:p.Ile904=
XM_005248618.4:c.2712A=	XP_005248675.1:p.Ile904=
XM_017010001.1:c.2565A=	XP_016865490.1:p.Ile855=
NM_001271769.2:c.2565A=	NP_001258698.1:p.Ile855=
NM_003664.5:c.2712A= MANE Select	NP_003655.3:p.Ile904=