Canonical Allele Identifier: CA2383551608
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891781T= , CM000683.2:g.25891781T= GRCh38
NC_000021.8:g.27264093T= , CM000683.1:g.27264093T= GRCh37
NC_000021.7:g.26185964T= NCBI36
NG_007376.1:g.284040A=
NG_007376.2:g.284348A=

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2152A= MANE Select ENSP00000284981.4:p.Ile718=
ENST00000346798.7:c.2152A= ENSP00000284981.4:p.Ile718=
ENST00000348990.9:c.1927A= ENSP00000345463.5:p.Ile643=
ENST00000354192.7:c.1759A= ENSP00000346129.3:p.Ile587=
ENST00000357903.7:c.2095A= ENSP00000350578.3:p.Ile699=
ENST00000358918.7:c.2098A= ENSP00000351796.3:p.Ile700=
ENST00000359726.7:c.1822A= ENSP00000352760.4:p.Ile608=
ENST00000439274.6:c.1984A= ENSP00000398879.2:p.Ile662=
ENST00000440126.7:c.2080A= ENSP00000387483.2:p.Ile694=
ENST00000464867.1:n.499A=
NM_000484.3:c.2152A= NP_000475.1:p.Ile718=
NM_001136016.3:c.2080A= NP_001129488.1:p.Ile694=
NM_001136129.2:c.1759A= NP_001129601.1:p.Ile587=
NM_001136130.2:c.1984A= NP_001129602.1:p.Ile662=
NM_001136131.2:c.1822A= NP_001129603.1:p.Ile608=
NM_001204301.1:c.2098A= NP_001191230.1:p.Ile700=
NM_001204302.1:c.2041A= NP_001191231.1:p.Ile681=
NM_001204303.1:c.1873A= NP_001191232.1:p.Ile625=
NM_201413.2:c.2095A= NP_958816.1:p.Ile699=
NM_201414.2:c.1927A= NP_958817.1:p.Ile643=
NM_000484.4:c.2152A= MANE Select NP_000475.1:p.Ile718=
NM_001136129.3:c.1759A= NP_001129601.1:p.Ile587=
NM_001136130.3:c.1984A= NP_001129602.1:p.Ile662=
NM_001204301.2:c.2098A= NP_001191230.1:p.Ile700=
NM_001204302.2:c.2041A= NP_001191231.1:p.Ile681=
NM_001204303.2:c.1873A= NP_001191232.1:p.Ile625=
NM_201413.3:c.2095A= NP_958816.1:p.Ile699=
NM_201414.3:c.1927A= NP_958817.1:p.Ile643=
NM_001136131.3:c.1822A= NP_001129603.1:p.Ile608=
NM_001385253.1:c.1984A= NP_001372182.1:p.Ile662=