Canonical Allele Identifier: CA409805711
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891867A>T , CM000683.2:g.25891867A>T GRCh38
NC_000021.8:g.27264179A>T , CM000683.1:g.27264179A>T GRCh37
NC_000021.7:g.26186050A>T NCBI36
NG_007376.1:g.283954T>A
NG_007376.2:g.284262T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2066T>A MANE Select ENSP00000284981.4:p.Val689Glu
ENST00000346798.7:c.2066T>A ENSP00000284981.4:p.Val689Glu
ENST00000348990.9:c.1841T>A ENSP00000345463.5:p.Val614Glu
ENST00000354192.7:c.1673T>A ENSP00000346129.3:p.Val558Glu
ENST00000357903.7:c.2009T>A ENSP00000350578.3:p.Val670Glu
ENST00000358918.7:c.2012T>A ENSP00000351796.3:p.Val671Glu
ENST00000359726.7:c.1736T>A ENSP00000352760.4:p.Val579Glu
ENST00000439274.6:c.1898T>A ENSP00000398879.2:p.Val633Glu
ENST00000440126.7:c.1994T>A ENSP00000387483.2:p.Val665Glu
NM_000484.3:c.2066T>A NP_000475.1:p.Val689Glu
NM_001136016.3:c.1994T>A NP_001129488.1:p.Val665Glu
NM_001136129.2:c.1673T>A NP_001129601.1:p.Val558Glu
NM_001136130.2:c.1898T>A NP_001129602.1:p.Val633Glu
NM_001136131.2:c.1736T>A NP_001129603.1:p.Val579Glu
NM_001204301.1:c.2012T>A NP_001191230.1:p.Val671Glu
NM_001204302.1:c.1955T>A NP_001191231.1:p.Val652Glu
NM_001204303.1:c.1787T>A NP_001191232.1:p.Val596Glu
NM_201413.2:c.2009T>A NP_958816.1:p.Val670Glu
NM_201414.2:c.1841T>A NP_958817.1:p.Val614Glu
NM_000484.4:c.2066T>A MANE Select NP_000475.1:p.Val689Glu
NM_001136129.3:c.1673T>A NP_001129601.1:p.Val558Glu
NM_001136130.3:c.1898T>A NP_001129602.1:p.Val633Glu
NM_001204301.2:c.2012T>A NP_001191230.1:p.Val671Glu
NM_001204302.2:c.1955T>A NP_001191231.1:p.Val652Glu
NM_001204303.2:c.1787T>A NP_001191232.1:p.Val596Glu
NM_201413.3:c.2009T>A NP_958816.1:p.Val670Glu
NM_201414.3:c.1841T>A NP_958817.1:p.Val614Glu
NM_001136131.3:c.1736T>A NP_001129603.1:p.Val579Glu
NM_001385253.1:c.1898T>A NP_001372182.1:p.Val633Glu