Canonical Allele Identifier: CA1779304522

Gene: AP3M2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42169450A= , CM000670.2:g.42169450A=	GRCh38
NC_000008.10:g.42026968A= , CM000670.1:g.42026968A=	GRCh37
NC_000008.9:g.42146125A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396926.8:c.*389A= MANE Select	ENSP00000380132.3:n.*389A=
ENST00000174653.3:c.*389A=	ENSP00000174653.3:n.*389A=
ENST00000396926.7:c.*389A=	ENSP00000380132.3:n.*389A=
ENST00000518421.5:c.*389A=	ENSP00000428787.1:n.*389A=
ENST00000520689.1:c.371+165A=	ENSP00000429804.1:n.371+165A=
NM_001134296.1:c.*389A=	NP_001127768.1:n.*389A=
NM_006803.3:c.*389A=	NP_006794.1:n.*389A=
XM_017012977.2:c.*389A=	XP_016868466.1:n.*389A=
XR_001745459.2:n.1931A=
NM_006803.4:c.*389A= MANE Select	NP_006794.1:n.*389A=
NM_001134296.2:c.*389A=	NP_001127768.1:n.*389A=