Canonical Allele Identifier: CA1779304695

Gene: AP3M2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42169816T= , CM000670.2:g.42169816T=	GRCh38
NC_000008.10:g.42027334T= , CM000670.1:g.42027334T=	GRCh37
NC_000008.9:g.42146491T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396926.8:c.*755T= MANE Select	ENSP00000380132.3:n.*755T=
ENST00000174653.3:c.*755T=	ENSP00000174653.3:n.*755T=
ENST00000396926.7:c.*755T=	ENSP00000380132.3:n.*755T=
ENST00000518421.5:c.*755T=	ENSP00000428787.1:n.*755T=
ENST00000520689.1:c.372-73T=	ENSP00000429804.1:n.372-73T=
NM_001134296.1:c.*755T=	NP_001127768.1:n.*755T=
NM_006803.3:c.*755T=	NP_006794.1:n.*755T=
XM_017012977.2:c.*755T=	XP_016868466.1:n.*755T=
XR_001745459.2:n.2297T=
NM_006803.4:c.*755T= MANE Select	NP_006794.1:n.*755T=
NM_001134296.2:c.*755T=	NP_001127768.1:n.*755T=