Canonical Allele Identifier: CA409806531
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897646T>A , CM000683.2:g.25897646T>A GRCh38
NC_000021.8:g.27269958T>A , CM000683.1:g.27269958T>A GRCh37
NC_000021.7:g.26191829T>A NCBI36
NG_007376.1:g.278175A>T
NG_007376.2:g.278483A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1958A>T
ENST00000707133.1:n.388A>T
ENST00000707134.1:n.657A>T
ENST00000346798.8:c.1991A>T MANE Select ENSP00000284981.4:p.Glu664Val
ENST00000346798.7:c.1991A>T ENSP00000284981.4:p.Glu664Val
ENST00000348990.9:c.1766A>T ENSP00000345463.5:p.Glu589Val
ENST00000354192.7:c.1598A>T ENSP00000346129.3:p.Glu533Val
ENST00000357903.7:c.1934A>T ENSP00000350578.3:p.Glu645Val
ENST00000358918.7:c.1937A>T ENSP00000351796.3:p.Glu646Val
ENST00000359726.7:c.1661A>T ENSP00000352760.4:p.Glu554Val
ENST00000439274.6:c.1823A>T ENSP00000398879.2:p.Glu608Val
ENST00000440126.7:c.1919A>T ENSP00000387483.2:p.Glu640Val
ENST00000464867.1:n.338A>T
NM_000484.3:c.1991A>T NP_000475.1:p.Glu664Val
NM_001136016.3:c.1919A>T NP_001129488.1:p.Glu640Val
NM_001136129.2:c.1598A>T NP_001129601.1:p.Glu533Val
NM_001136130.2:c.1823A>T NP_001129602.1:p.Glu608Val
NM_001136131.2:c.1661A>T NP_001129603.1:p.Glu554Val
NM_001204301.1:c.1937A>T NP_001191230.1:p.Glu646Val
NM_001204302.1:c.1880A>T NP_001191231.1:p.Glu627Val
NM_001204303.1:c.1712A>T NP_001191232.1:p.Glu571Val
NM_201413.2:c.1934A>T NP_958816.1:p.Glu645Val
NM_201414.2:c.1766A>T NP_958817.1:p.Glu589Val
NM_000484.4:c.1991A>T MANE Select NP_000475.1:p.Glu664Val
NM_001136129.3:c.1598A>T NP_001129601.1:p.Glu533Val
NM_001136130.3:c.1823A>T NP_001129602.1:p.Glu608Val
NM_001204301.2:c.1937A>T NP_001191230.1:p.Glu646Val
NM_001204302.2:c.1880A>T NP_001191231.1:p.Glu627Val
NM_001204303.2:c.1712A>T NP_001191232.1:p.Glu571Val
NM_201413.3:c.1934A>T NP_958816.1:p.Glu645Val
NM_201414.3:c.1766A>T NP_958817.1:p.Glu589Val
NM_001136131.3:c.1661A>T NP_001129603.1:p.Glu554Val
NM_001385253.1:c.1823A>T NP_001372182.1:p.Glu608Val