Canonical Allele Identifier: CA1779304533

Gene: AP3M2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42169478A= , CM000670.2:g.42169478A=	GRCh38
NC_000008.10:g.42026996A= , CM000670.1:g.42026996A=	GRCh37
NC_000008.9:g.42146153A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396926.8:c.*417A= MANE Select	ENSP00000380132.3:n.*417A=
ENST00000174653.3:c.*417A=	ENSP00000174653.3:n.*417A=
ENST00000396926.7:c.*417A=	ENSP00000380132.3:n.*417A=
ENST00000518421.5:c.*417A=	ENSP00000428787.1:n.*417A=
ENST00000520689.1:c.371+193A=	ENSP00000429804.1:n.371+193A=
NM_001134296.1:c.*417A=	NP_001127768.1:n.*417A=
NM_006803.3:c.*417A=	NP_006794.1:n.*417A=
XM_017012977.2:c.*417A=	XP_016868466.1:n.*417A=
XR_001745459.2:n.1959A=
NM_006803.4:c.*417A= MANE Select	NP_006794.1:n.*417A=
NM_001134296.2:c.*417A=	NP_001127768.1:n.*417A=