Canonical Allele Identifier: CA2383551605

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891765A= , CM000683.2:g.25891765A=	GRCh38
NC_000021.8:g.27264077A= , CM000683.1:g.27264077A=	GRCh37
NC_000021.7:g.26185948A=	NCBI36
NG_007376.1:g.284056T=
NG_007376.2:g.284364T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2135T=
ENST00000707133.1:n.565T=
ENST00000707134.1:n.834T=
ENST00000346798.8:c.2168T= MANE Select	ENSP00000284981.4:p.Leu723=
ENST00000346798.7:c.2168T=	ENSP00000284981.4:p.Leu723=
ENST00000348990.9:c.1943T=	ENSP00000345463.5:p.Leu648=
ENST00000354192.7:c.1775T=	ENSP00000346129.3:p.Leu592=
ENST00000357903.7:c.2111T=	ENSP00000350578.3:p.Leu704=
ENST00000358918.7:c.2114T=	ENSP00000351796.3:p.Leu705=
ENST00000359726.7:c.1838T=	ENSP00000352760.4:p.Leu613=
ENST00000439274.6:c.2000T=	ENSP00000398879.2:p.Leu667=
ENST00000440126.7:c.2096T=	ENSP00000387483.2:p.Leu699=
ENST00000464867.1:n.515T=
NM_000484.3:c.2168T=	NP_000475.1:p.Leu723=
NM_001136016.3:c.2096T=	NP_001129488.1:p.Leu699=
NM_001136129.2:c.1775T=	NP_001129601.1:p.Leu592=
NM_001136130.2:c.2000T=	NP_001129602.1:p.Leu667=
NM_001136131.2:c.1838T=	NP_001129603.1:p.Leu613=
NM_001204301.1:c.2114T=	NP_001191230.1:p.Leu705=
NM_001204302.1:c.2057T=	NP_001191231.1:p.Leu686=
NM_001204303.1:c.1889T=	NP_001191232.1:p.Leu630=
NM_201413.2:c.2111T=	NP_958816.1:p.Leu704=
NM_201414.2:c.1943T=	NP_958817.1:p.Leu648=
NM_000484.4:c.2168T= MANE Select	NP_000475.1:p.Leu723=
NM_001136129.3:c.1775T=	NP_001129601.1:p.Leu592=
NM_001136130.3:c.2000T=	NP_001129602.1:p.Leu667=
NM_001204301.2:c.2114T=	NP_001191230.1:p.Leu705=
NM_001204302.2:c.2057T=	NP_001191231.1:p.Leu686=
NM_001204303.2:c.1889T=	NP_001191232.1:p.Leu630=
NM_201413.3:c.2111T=	NP_958816.1:p.Leu704=
NM_201414.3:c.1943T=	NP_958817.1:p.Leu648=
NM_001136131.3:c.1838T=	NP_001129603.1:p.Leu613=
NM_001385253.1:c.2000T=	NP_001372182.1:p.Leu667=