Canonical Allele Identifier: CA360187934

Gene: AP3B1

Linked Data

• MyVariant Identifiers: chr5:g.77425049C>G (hg19) ; chr5:g.78129225C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78129225C>G , CM000667.2:g.78129225C>G	GRCh38
NC_000005.9:g.77425049C>G , CM000667.1:g.77425049C>G	GRCh37
NC_000005.8:g.77460805C>G	NCBI36
NG_007268.1:g.170480G>C , LRG_170:g.170480G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000517561.2:c.1733G>C	ENSP00000511839.1:p.Arg578Thr
ENST00000517940.2:c.1733G>C	ENSP00000511881.1:p.Arg578Thr
ENST00000519295.6:c.1586G>C	ENSP00000430597.1:p.Arg529Thr
ENST00000519888.6:c.1733G>C	ENSP00000511880.1:p.Arg578Thr
ENST00000695447.1:c.1733G>C	ENSP00000511917.1:p.Arg578Thr
ENST00000695450.1:c.1168-12991G>C	ENSP00000511919.1:n.1168-12991G>C
ENST00000695451.1:c.*1499G>C	ENSP00000511920.1:n.*1499G>C
ENST00000695453.1:c.1676G>C	ENSP00000511921.1:p.Arg559Thr
ENST00000695454.1:c.1727G>C	ENSP00000511922.1:p.Arg576Thr
ENST00000695455.1:c.1586G>C	ENSP00000511923.1:p.Arg529Thr
ENST00000695488.1:c.1733G>C	ENSP00000511959.1:p.Arg578Thr
ENST00000695505.1:n.1891G>C
ENST00000695507.1:c.1733G>C	ENSP00000511970.1:p.Arg578Thr
ENST00000695510.1:c.1733G>C	ENSP00000511973.1:p.Arg578Thr
ENST00000695511.1:c.1733G>C	ENSP00000511974.1:p.Arg578Thr
ENST00000695512.1:c.1733G>C	ENSP00000511975.1:p.Arg578Thr
ENST00000695513.1:c.1598G>C	ENSP00000511976.1:p.Arg533Thr
ENST00000695514.1:c.1733G>C	ENSP00000511977.1:p.Arg578Thr
ENST00000695515.1:c.1733G>C	ENSP00000511978.1:p.Arg578Thr
ENST00000255194.11:c.1733G>C MANE Select	ENSP00000255194.7:p.Arg578Thr
ENST00000255194.10:c.1733G>C	ENSP00000255194.6:p.Arg578Thr
ENST00000517561.1:n.111G>C
ENST00000519295.5:c.1586G>C	ENSP00000430597.1:p.Arg529Thr
NM_001271769.1:c.1586G>C	NP_001258698.1:p.Arg529Thr
NM_003664.4:c.1733G>C , LRG_170t1:c.1733G>C	NP_003655.3:p.Arg578Thr
XM_005248618.2:c.1733G>C	XP_005248675.1:p.Arg578Thr
XM_005248619.3:c.1733G>C	XP_005248676.1:p.Arg578Thr
XM_005248618.4:c.1733G>C	XP_005248675.1:p.Arg578Thr
XM_005248619.5:c.1733G>C	XP_005248676.1:p.Arg578Thr
XM_017010001.1:c.1586G>C	XP_016865490.1:p.Arg529Thr
NM_001271769.2:c.1586G>C	NP_001258698.1:p.Arg529Thr
NM_003664.5:c.1733G>C MANE Select	NP_003655.3:p.Arg578Thr