Canonical Allele Identifier: CA409805413
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891723T>A , CM000683.2:g.25891723T>A GRCh38
NC_000021.8:g.27264035T>A , CM000683.1:g.27264035T>A GRCh37
NC_000021.7:g.26185906T>A NCBI36
NG_007376.1:g.284098A>T
NG_007376.2:g.284406A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2210A>T MANE Select ENSP00000284981.4:p.Glu737Val
ENST00000346798.7:c.2210A>T ENSP00000284981.4:p.Glu737Val
ENST00000348990.9:c.1985A>T ENSP00000345463.5:p.Glu662Val
ENST00000354192.7:c.1817A>T ENSP00000346129.3:p.Glu606Val
ENST00000357903.7:c.2153A>T ENSP00000350578.3:p.Glu718Val
ENST00000358918.7:c.2156A>T ENSP00000351796.3:p.Glu719Val
ENST00000359726.7:c.1880A>T ENSP00000352760.4:p.Glu627Val
ENST00000439274.6:c.2042A>T ENSP00000398879.2:p.Glu681Val
ENST00000440126.7:c.2138A>T ENSP00000387483.2:p.Glu713Val
ENST00000464867.1:n.557A>T
NM_000484.3:c.2210A>T NP_000475.1:p.Glu737Val
NM_001136016.3:c.2138A>T NP_001129488.1:p.Glu713Val
NM_001136129.2:c.1817A>T NP_001129601.1:p.Glu606Val
NM_001136130.2:c.2042A>T NP_001129602.1:p.Glu681Val
NM_001136131.2:c.1880A>T NP_001129603.1:p.Glu627Val
NM_001204301.1:c.2156A>T NP_001191230.1:p.Glu719Val
NM_001204302.1:c.2099A>T NP_001191231.1:p.Glu700Val
NM_001204303.1:c.1931A>T NP_001191232.1:p.Glu644Val
NM_201413.2:c.2153A>T NP_958816.1:p.Glu718Val
NM_201414.2:c.1985A>T NP_958817.1:p.Glu662Val
NM_000484.4:c.2210A>T MANE Select NP_000475.1:p.Glu737Val
NM_001136129.3:c.1817A>T NP_001129601.1:p.Glu606Val
NM_001136130.3:c.2042A>T NP_001129602.1:p.Glu681Val
NM_001204301.2:c.2156A>T NP_001191230.1:p.Glu719Val
NM_001204302.2:c.2099A>T NP_001191231.1:p.Glu700Val
NM_001204303.2:c.1931A>T NP_001191232.1:p.Glu644Val
NM_201413.3:c.2153A>T NP_958816.1:p.Glu718Val
NM_201414.3:c.1985A>T NP_958817.1:p.Glu662Val
NM_001136131.3:c.1880A>T NP_001129603.1:p.Glu627Val
NM_001385253.1:c.2042A>T NP_001372182.1:p.Glu681Val