Canonical Allele Identifier: CA2383554911

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897593C= , CM000683.2:g.25897593C=	GRCh38
NC_000021.8:g.27269905C= , CM000683.1:g.27269905C=	GRCh37
NC_000021.7:g.26191776C=	NCBI36
NG_007376.1:g.278228G=
NG_007376.2:g.278536G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2011G=
ENST00000707133.1:n.441G=
ENST00000707134.1:n.710G=
ENST00000346798.8:c.2044G= MANE Select	ENSP00000284981.4:p.Glu682=
ENST00000346798.7:c.2044G=	ENSP00000284981.4:p.Glu682=
ENST00000348990.9:c.1819G=	ENSP00000345463.5:p.Glu607=
ENST00000354192.7:c.1651G=	ENSP00000346129.3:p.Glu551=
ENST00000357903.7:c.1987G=	ENSP00000350578.3:p.Glu663=
ENST00000358918.7:c.1990G=	ENSP00000351796.3:p.Glu664=
ENST00000359726.7:c.1714G=	ENSP00000352760.4:p.Glu572=
ENST00000439274.6:c.1876G=	ENSP00000398879.2:p.Glu626=
ENST00000440126.7:c.1972G=	ENSP00000387483.2:p.Glu658=
ENST00000464867.1:n.391G=
NM_000484.3:c.2044G=	NP_000475.1:p.Glu682=
NM_001136016.3:c.1972G=	NP_001129488.1:p.Glu658=
NM_001136129.2:c.1651G=	NP_001129601.1:p.Glu551=
NM_001136130.2:c.1876G=	NP_001129602.1:p.Glu626=
NM_001136131.2:c.1714G=	NP_001129603.1:p.Glu572=
NM_001204301.1:c.1990G=	NP_001191230.1:p.Glu664=
NM_001204302.1:c.1933G=	NP_001191231.1:p.Glu645=
NM_001204303.1:c.1765G=	NP_001191232.1:p.Glu589=
NM_201413.2:c.1987G=	NP_958816.1:p.Glu663=
NM_201414.2:c.1819G=	NP_958817.1:p.Glu607=
NM_000484.4:c.2044G= MANE Select	NP_000475.1:p.Glu682=
NM_001136129.3:c.1651G=	NP_001129601.1:p.Glu551=
NM_001136130.3:c.1876G=	NP_001129602.1:p.Glu626=
NM_001204301.2:c.1990G=	NP_001191230.1:p.Glu664=
NM_001204302.2:c.1933G=	NP_001191231.1:p.Glu645=
NM_001204303.2:c.1765G=	NP_001191232.1:p.Glu589=
NM_201413.3:c.1987G=	NP_958816.1:p.Glu663=
NM_201414.3:c.1819G=	NP_958817.1:p.Glu607=
NM_001136131.3:c.1714G=	NP_001129603.1:p.Glu572=
NM_001385253.1:c.1876G=	NP_001372182.1:p.Glu626=