Canonical Allele Identifier: CA2383551599

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891735T= , CM000683.2:g.25891735T=	GRCh38
NC_000021.8:g.27264047T= , CM000683.1:g.27264047T=	GRCh37
NC_000021.7:g.26185918T=	NCBI36
NG_007376.1:g.284086A=
NG_007376.2:g.284394A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2165A=
ENST00000707133.1:n.595A=
ENST00000707134.1:n.864A=
ENST00000346798.8:c.2198A= MANE Select	ENSP00000284981.4:p.His733=
ENST00000346798.7:c.2198A=	ENSP00000284981.4:p.His733=
ENST00000348990.9:c.1973A=	ENSP00000345463.5:p.His658=
ENST00000354192.7:c.1805A=	ENSP00000346129.3:p.His602=
ENST00000357903.7:c.2141A=	ENSP00000350578.3:p.His714=
ENST00000358918.7:c.2144A=	ENSP00000351796.3:p.His715=
ENST00000359726.7:c.1868A=	ENSP00000352760.4:p.His623=
ENST00000439274.6:c.2030A=	ENSP00000398879.2:p.His677=
ENST00000440126.7:c.2126A=	ENSP00000387483.2:p.His709=
ENST00000464867.1:n.545A=
NM_000484.3:c.2198A=	NP_000475.1:p.His733=
NM_001136016.3:c.2126A=	NP_001129488.1:p.His709=
NM_001136129.2:c.1805A=	NP_001129601.1:p.His602=
NM_001136130.2:c.2030A=	NP_001129602.1:p.His677=
NM_001136131.2:c.1868A=	NP_001129603.1:p.His623=
NM_001204301.1:c.2144A=	NP_001191230.1:p.His715=
NM_001204302.1:c.2087A=	NP_001191231.1:p.His696=
NM_001204303.1:c.1919A=	NP_001191232.1:p.His640=
NM_201413.2:c.2141A=	NP_958816.1:p.His714=
NM_201414.2:c.1973A=	NP_958817.1:p.His658=
NM_000484.4:c.2198A= MANE Select	NP_000475.1:p.His733=
NM_001136129.3:c.1805A=	NP_001129601.1:p.His602=
NM_001136130.3:c.2030A=	NP_001129602.1:p.His677=
NM_001204301.2:c.2144A=	NP_001191230.1:p.His715=
NM_001204302.2:c.2087A=	NP_001191231.1:p.His696=
NM_001204303.2:c.1919A=	NP_001191232.1:p.His640=
NM_201413.3:c.2141A=	NP_958816.1:p.His714=
NM_201414.3:c.1973A=	NP_958817.1:p.His658=
NM_001136131.3:c.1868A=	NP_001129603.1:p.His623=
NM_001385253.1:c.2030A=	NP_001372182.1:p.His677=