Canonical Allele Identifier: CA360331897

Gene: AP3B1

Linked Data

• MyVariant Identifiers: chr5:g.77334892C>T (hg19) ; chr5:g.78039068C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78039068C>T , CM000667.2:g.78039068C>T	GRCh38
NC_000005.9:g.77334892C>T , CM000667.1:g.77334892C>T	GRCh37
NC_000005.8:g.77370648C>T	NCBI36
NG_007268.1:g.260637G>A , LRG_170:g.260637G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519295.6:c.2637G>A	ENSP00000430597.1:p.Met879Ile
ENST00000523204.2:n.584G>A
ENST00000695447.1:c.2677G>A	ENSP00000511917.1:n.2677G>A
ENST00000695450.1:c.1983G>A	ENSP00000511919.1:p.Met661Ile
ENST00000695451.1:c.*2546G>A	ENSP00000511920.1:n.*2546G>A
ENST00000695453.1:c.2727G>A	ENSP00000511921.1:p.Met909Ile
ENST00000695454.1:c.2778G>A	ENSP00000511922.1:p.Met926Ile
ENST00000695455.1:c.2637G>A	ENSP00000511923.1:p.Met879Ile
ENST00000695458.1:n.499G>A
ENST00000695488.1:c.2784G>A	ENSP00000511959.1:p.Met928Ile
ENST00000695505.1:n.2942G>A
ENST00000695506.1:n.436G>A
ENST00000695507.1:c.*309G>A	ENSP00000511970.1:n.*309G>A
ENST00000695510.1:c.2784G>A	ENSP00000511973.1:p.Met928Ile
ENST00000695511.1:c.2784G>A	ENSP00000511974.1:p.Met928Ile
ENST00000695512.1:c.2604G>A	ENSP00000511975.1:p.Met868Ile
ENST00000695513.1:c.2649G>A	ENSP00000511976.1:p.Met883Ile
ENST00000695515.1:c.2784G>A	ENSP00000511978.1:p.Met928Ile
ENST00000255194.11:c.2784G>A MANE Select	ENSP00000255194.7:p.Met928Ile
ENST00000255194.10:c.2784G>A	ENSP00000255194.6:p.Met928Ile
ENST00000519295.5:c.2637G>A	ENSP00000430597.1:p.Met879Ile
ENST00000522901.1:c.83G>A
ENST00000523204.1:n.584G>A
NM_001271769.1:c.2637G>A	NP_001258698.1:p.Met879Ile
NM_003664.4:c.2784G>A , LRG_170t1:c.2784G>A	NP_003655.3:p.Met928Ile
XM_005248618.2:c.2784G>A	XP_005248675.1:p.Met928Ile
XM_005248618.4:c.2784G>A	XP_005248675.1:p.Met928Ile
XM_017010001.1:c.2637G>A	XP_016865490.1:p.Met879Ile
NM_001271769.2:c.2637G>A	NP_001258698.1:p.Met879Ile
NM_003664.5:c.2784G>A MANE Select	NP_003655.3:p.Met928Ile