Canonical Allele Identifier: CA1779304539

Gene: AP3M2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42169482G= , CM000670.2:g.42169482G=	GRCh38
NC_000008.10:g.42027000G= , CM000670.1:g.42027000G=	GRCh37
NC_000008.9:g.42146157G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396926.8:c.*421G= MANE Select	ENSP00000380132.3:n.*421G=
ENST00000174653.3:c.*421G=	ENSP00000174653.3:n.*421G=
ENST00000396926.7:c.*421G=	ENSP00000380132.3:n.*421G=
ENST00000518421.5:c.*421G=	ENSP00000428787.1:n.*421G=
ENST00000520689.1:c.371+197G=	ENSP00000429804.1:n.371+197G=
NM_001134296.1:c.*421G=	NP_001127768.1:n.*421G=
NM_006803.3:c.*421G=	NP_006794.1:n.*421G=
XM_017012977.2:c.*421G=	XP_016868466.1:n.*421G=
XR_001745459.2:n.1963G=
NM_006803.4:c.*421G= MANE Select	NP_006794.1:n.*421G=
NM_001134296.2:c.*421G=	NP_001127768.1:n.*421G=