Canonical Allele Identifier: CA2383554901

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897576T= , CM000683.2:g.25897576T=	GRCh38
NC_000021.8:g.27269888T= , CM000683.1:g.27269888T=	GRCh37
NC_000021.7:g.26191759T=	NCBI36
NG_007376.1:g.278245A=
NG_007376.2:g.278553A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2028A=
ENST00000707133.1:n.458A=
ENST00000707134.1:n.727A=
ENST00000346798.8:c.2061A= MANE Select	ENSP00000284981.4:p.Lys687=
ENST00000346798.7:c.2061A=	ENSP00000284981.4:p.Lys687=
ENST00000348990.9:c.1836A=	ENSP00000345463.5:p.Lys612=
ENST00000354192.7:c.1668A=	ENSP00000346129.3:p.Lys556=
ENST00000357903.7:c.2004A=	ENSP00000350578.3:p.Lys668=
ENST00000358918.7:c.2007A=	ENSP00000351796.3:p.Lys669=
ENST00000359726.7:c.1731A=	ENSP00000352760.4:p.Lys577=
ENST00000439274.6:c.1893A=	ENSP00000398879.2:p.Lys631=
ENST00000440126.7:c.1989A=	ENSP00000387483.2:p.Lys663=
ENST00000464867.1:n.408A=
NM_000484.3:c.2061A=	NP_000475.1:p.Lys687=
NM_001136016.3:c.1989A=	NP_001129488.1:p.Lys663=
NM_001136129.2:c.1668A=	NP_001129601.1:p.Lys556=
NM_001136130.2:c.1893A=	NP_001129602.1:p.Lys631=
NM_001136131.2:c.1731A=	NP_001129603.1:p.Lys577=
NM_001204301.1:c.2007A=	NP_001191230.1:p.Lys669=
NM_001204302.1:c.1950A=	NP_001191231.1:p.Lys650=
NM_001204303.1:c.1782A=	NP_001191232.1:p.Lys594=
NM_201413.2:c.2004A=	NP_958816.1:p.Lys668=
NM_201414.2:c.1836A=	NP_958817.1:p.Lys612=
NM_000484.4:c.2061A= MANE Select	NP_000475.1:p.Lys687=
NM_001136129.3:c.1668A=	NP_001129601.1:p.Lys556=
NM_001136130.3:c.1893A=	NP_001129602.1:p.Lys631=
NM_001204301.2:c.2007A=	NP_001191230.1:p.Lys669=
NM_001204302.2:c.1950A=	NP_001191231.1:p.Lys650=
NM_001204303.2:c.1782A=	NP_001191232.1:p.Lys594=
NM_201413.3:c.2004A=	NP_958816.1:p.Lys668=
NM_201414.3:c.1836A=	NP_958817.1:p.Lys612=
NM_001136131.3:c.1731A=	NP_001129603.1:p.Lys577=
NM_001385253.1:c.1893A=	NP_001372182.1:p.Lys631=