Canonical Allele Identifier: CA1779304453

Gene: AP3M2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42169282C= , CM000670.2:g.42169282C=	GRCh38
NC_000008.10:g.42026800C= , CM000670.1:g.42026800C=	GRCh37
NC_000008.9:g.42145957C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396926.8:c.*221C= MANE Select	ENSP00000380132.3:n.*221C=
ENST00000174653.3:c.*221C=	ENSP00000174653.3:n.*221C=
ENST00000396926.7:c.*221C=	ENSP00000380132.3:n.*221C=
ENST00000518421.5:c.*221C=	ENSP00000428787.1:n.*221C=
ENST00000520689.1:c.368C=	ENSP00000429804.1:n.368C=
NM_001134296.1:c.*221C=	NP_001127768.1:n.*221C=
NM_006803.3:c.*221C=	NP_006794.1:n.*221C=
XM_017012977.2:c.*221C=	XP_016868466.1:n.*221C=
XR_001745459.2:n.1763C=
NM_006803.4:c.*221C= MANE Select	NP_006794.1:n.*221C=
NM_001134296.2:c.*221C=	NP_001127768.1:n.*221C=