Canonical Allele Identifier: CA2383551647
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891858G= , CM000683.2:g.25891858G= GRCh38
NC_000021.8:g.27264170G= , CM000683.1:g.27264170G= GRCh37
NC_000021.7:g.26186041G= NCBI36
NG_007376.1:g.283963C=
NG_007376.2:g.284271C=

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2042C=
ENST00000707133.1:n.472C=
ENST00000707134.1:n.741C=
ENST00000346798.8:c.2075C= MANE Select ENSP00000284981.4:p.Ala692=
ENST00000346798.7:c.2075C= ENSP00000284981.4:p.Ala692=
ENST00000348990.9:c.1850C= ENSP00000345463.5:p.Ala617=
ENST00000354192.7:c.1682C= ENSP00000346129.3:p.Ala561=
ENST00000357903.7:c.2018C= ENSP00000350578.3:p.Ala673=
ENST00000358918.7:c.2021C= ENSP00000351796.3:p.Ala674=
ENST00000359726.7:c.1745C= ENSP00000352760.4:p.Ala582=
ENST00000439274.6:c.1907C= ENSP00000398879.2:p.Ala636=
ENST00000440126.7:c.2003C= ENSP00000387483.2:p.Ala668=
ENST00000464867.1:n.422C=
NM_000484.3:c.2075C= NP_000475.1:p.Ala692=
NM_001136016.3:c.2003C= NP_001129488.1:p.Ala668=
NM_001136129.2:c.1682C= NP_001129601.1:p.Ala561=
NM_001136130.2:c.1907C= NP_001129602.1:p.Ala636=
NM_001136131.2:c.1745C= NP_001129603.1:p.Ala582=
NM_001204301.1:c.2021C= NP_001191230.1:p.Ala674=
NM_001204302.1:c.1964C= NP_001191231.1:p.Ala655=
NM_001204303.1:c.1796C= NP_001191232.1:p.Ala599=
NM_201413.2:c.2018C= NP_958816.1:p.Ala673=
NM_201414.2:c.1850C= NP_958817.1:p.Ala617=
NM_000484.4:c.2075C= MANE Select NP_000475.1:p.Ala692=
NM_001136129.3:c.1682C= NP_001129601.1:p.Ala561=
NM_001136130.3:c.1907C= NP_001129602.1:p.Ala636=
NM_001204301.2:c.2021C= NP_001191230.1:p.Ala674=
NM_001204302.2:c.1964C= NP_001191231.1:p.Ala655=
NM_001204303.2:c.1796C= NP_001191232.1:p.Ala599=
NM_201413.3:c.2018C= NP_958816.1:p.Ala673=
NM_201414.3:c.1850C= NP_958817.1:p.Ala617=
NM_001136131.3:c.1745C= NP_001129603.1:p.Ala582=
NM_001385253.1:c.1907C= NP_001372182.1:p.Ala636=