Canonical Allele Identifier: CA1779304674

Gene: AP3M2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42169780A= , CM000670.2:g.42169780A=	GRCh38
NC_000008.10:g.42027298A= , CM000670.1:g.42027298A=	GRCh37
NC_000008.9:g.42146455A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396926.8:c.*719A= MANE Select	ENSP00000380132.3:n.*719A=
ENST00000174653.3:c.*719A=	ENSP00000174653.3:n.*719A=
ENST00000396926.7:c.*719A=	ENSP00000380132.3:n.*719A=
ENST00000518421.5:c.*719A=	ENSP00000428787.1:n.*719A=
ENST00000520689.1:c.372-109A=	ENSP00000429804.1:n.372-109A=
NM_001134296.1:c.*719A=	NP_001127768.1:n.*719A=
NM_006803.3:c.*719A=	NP_006794.1:n.*719A=
XM_017012977.2:c.*719A=	XP_016868466.1:n.*719A=
XR_001745459.2:n.2261A=
NM_006803.4:c.*719A= MANE Select	NP_006794.1:n.*719A=
NM_001134296.2:c.*719A=	NP_001127768.1:n.*719A=