Canonical Allele Identifier: CA2383551613
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891786A= , CM000683.2:g.25891786A= GRCh38
NC_000021.8:g.27264098A= , CM000683.1:g.27264098A= GRCh37
NC_000021.7:g.26185969A= NCBI36
NG_007376.1:g.284035T=
NG_007376.2:g.284343T=

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2114T=
ENST00000707133.1:n.544T=
ENST00000707134.1:n.813T=
ENST00000346798.8:c.2147T= MANE Select ENSP00000284981.4:p.Ile716=
ENST00000346798.7:c.2147T= ENSP00000284981.4:p.Ile716=
ENST00000348990.9:c.1922T= ENSP00000345463.5:p.Ile641=
ENST00000354192.7:c.1754T= ENSP00000346129.3:p.Ile585=
ENST00000357903.7:c.2090T= ENSP00000350578.3:p.Ile697=
ENST00000358918.7:c.2093T= ENSP00000351796.3:p.Ile698=
ENST00000359726.7:c.1817T= ENSP00000352760.4:p.Ile606=
ENST00000439274.6:c.1979T= ENSP00000398879.2:p.Ile660=
ENST00000440126.7:c.2075T= ENSP00000387483.2:p.Ile692=
ENST00000464867.1:n.494T=
NM_000484.3:c.2147T= NP_000475.1:p.Ile716=
NM_001136016.3:c.2075T= NP_001129488.1:p.Ile692=
NM_001136129.2:c.1754T= NP_001129601.1:p.Ile585=
NM_001136130.2:c.1979T= NP_001129602.1:p.Ile660=
NM_001136131.2:c.1817T= NP_001129603.1:p.Ile606=
NM_001204301.1:c.2093T= NP_001191230.1:p.Ile698=
NM_001204302.1:c.2036T= NP_001191231.1:p.Ile679=
NM_001204303.1:c.1868T= NP_001191232.1:p.Ile623=
NM_201413.2:c.2090T= NP_958816.1:p.Ile697=
NM_201414.2:c.1922T= NP_958817.1:p.Ile641=
NM_000484.4:c.2147T= MANE Select NP_000475.1:p.Ile716=
NM_001136129.3:c.1754T= NP_001129601.1:p.Ile585=
NM_001136130.3:c.1979T= NP_001129602.1:p.Ile660=
NM_001204301.2:c.2093T= NP_001191230.1:p.Ile698=
NM_001204302.2:c.2036T= NP_001191231.1:p.Ile679=
NM_001204303.2:c.1868T= NP_001191232.1:p.Ile623=
NM_201413.3:c.2090T= NP_958816.1:p.Ile697=
NM_201414.3:c.1922T= NP_958817.1:p.Ile641=
NM_001136131.3:c.1817T= NP_001129603.1:p.Ile606=
NM_001385253.1:c.1979T= NP_001372182.1:p.Ile660=