Canonical Allele Identifier: CA1779304631

Gene: AP3M2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42169690T= , CM000670.2:g.42169690T=	GRCh38
NC_000008.10:g.42027208T= , CM000670.1:g.42027208T=	GRCh37
NC_000008.9:g.42146365T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000396926.8:c.*629T= MANE Select	ENSP00000380132.3:n.*629T=
ENST00000174653.3:c.*629T=	ENSP00000174653.3:n.*629T=
ENST00000396926.7:c.*629T=	ENSP00000380132.3:n.*629T=
ENST00000518421.5:c.*629T=	ENSP00000428787.1:n.*629T=
ENST00000520689.1:c.372-199T=	ENSP00000429804.1:n.372-199T=
NM_001134296.1:c.*629T=	NP_001127768.1:n.*629T=
NM_006803.3:c.*629T=	NP_006794.1:n.*629T=
XM_017012977.2:c.*629T=	XP_016868466.1:n.*629T=
XR_001745459.2:n.2171T=
NM_006803.4:c.*629T= MANE Select	NP_006794.1:n.*629T=
NM_001134296.2:c.*629T=	NP_001127768.1:n.*629T=