Canonical Allele Identifier: CA371085423

Gene: AP3M2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42165093C>G , CM000670.2:g.42165093C>G	GRCh38
NC_000008.10:g.42022611C>G , CM000670.1:g.42022611C>G	GRCh37
NC_000008.9:g.42141768C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006803.4:c.606C>G MANE Select	NP_006794.1:p.Ile202Met
ENST00000396926.8:c.606C>G MANE Select	ENSP00000380132.3:p.Ile202Met
NM_001134296.1:c.606C>G	NP_001127768.1:p.Ile202Met
NM_001134296.2:c.606C>G	NP_001127768.1:p.Ile202Met
NM_006803.3:c.606C>G	NP_006794.1:p.Ile202Met
ENST00000174653.3:c.606C>G	ENSP00000174653.3:p.Ile202Met
ENST00000396926.7:c.606C>G	ENSP00000380132.3:p.Ile202Met
ENST00000517499.5:c.195C>G	ENSP00000429037.1:p.Ile65Met
ENST00000517865.5:c.*337C>G	ENSP00000430200.1:n.*337C>G
ENST00000517922.5:c.606C>G	ENSP00000429435.1:p.Ile202Met
ENST00000518421.5:c.606C>G	ENSP00000428787.1:p.Ile202Met
ENST00000520685.1:n.78-2573C>G
ENST00000521280.5:c.261C>G	ENSP00000430616.1:p.Ile87Met
ENST00000521899.1:n.373C>G
ENST00000523249.1:n.611C>G
ENST00000530375.5:c.606C>G	ENSP00000431918.1:p.Ile202Met
XM_017012977.2:c.606C>G	XP_016868466.1:p.Ile202Met
XR_001745459.2:n.749C>G