Canonical Allele Identifier: CA1779304662

Gene: AP3M2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42169759G= , CM000670.2:g.42169759G=	GRCh38
NC_000008.10:g.42027277G= , CM000670.1:g.42027277G=	GRCh37
NC_000008.9:g.42146434G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000396926.8:c.*698G= MANE Select	ENSP00000380132.3:n.*698G=
ENST00000174653.3:c.*698G=	ENSP00000174653.3:n.*698G=
ENST00000396926.7:c.*698G=	ENSP00000380132.3:n.*698G=
ENST00000518421.5:c.*698G=	ENSP00000428787.1:n.*698G=
ENST00000520689.1:c.372-130G=	ENSP00000429804.1:n.372-130G=
NM_001134296.1:c.*698G=	NP_001127768.1:n.*698G=
NM_006803.3:c.*698G=	NP_006794.1:n.*698G=
XM_017012977.2:c.*698G=	XP_016868466.1:n.*698G=
XR_001745459.2:n.2240G=
NM_006803.4:c.*698G= MANE Select	NP_006794.1:n.*698G=
NM_001134296.2:c.*698G=	NP_001127768.1:n.*698G=