Canonical Allele Identifier: CA409805707
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891865A>C , CM000683.2:g.25891865A>C GRCh38
NC_000021.8:g.27264177A>C , CM000683.1:g.27264177A>C GRCh37
NC_000021.7:g.26186048A>C NCBI36
NG_007376.1:g.283956T>G
NG_007376.2:g.284264T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2068T>G MANE Select ENSP00000284981.4:p.Phe690Val
ENST00000346798.7:c.2068T>G ENSP00000284981.4:p.Phe690Val
ENST00000348990.9:c.1843T>G ENSP00000345463.5:p.Phe615Val
ENST00000354192.7:c.1675T>G ENSP00000346129.3:p.Phe559Val
ENST00000357903.7:c.2011T>G ENSP00000350578.3:p.Phe671Val
ENST00000358918.7:c.2014T>G ENSP00000351796.3:p.Phe672Val
ENST00000359726.7:c.1738T>G ENSP00000352760.4:p.Phe580Val
ENST00000439274.6:c.1900T>G ENSP00000398879.2:p.Phe634Val
ENST00000440126.7:c.1996T>G ENSP00000387483.2:p.Phe666Val
ENST00000464867.1:n.415T>G
NM_000484.3:c.2068T>G NP_000475.1:p.Phe690Val
NM_001136016.3:c.1996T>G NP_001129488.1:p.Phe666Val
NM_001136129.2:c.1675T>G NP_001129601.1:p.Phe559Val
NM_001136130.2:c.1900T>G NP_001129602.1:p.Phe634Val
NM_001136131.2:c.1738T>G NP_001129603.1:p.Phe580Val
NM_001204301.1:c.2014T>G NP_001191230.1:p.Phe672Val
NM_001204302.1:c.1957T>G NP_001191231.1:p.Phe653Val
NM_001204303.1:c.1789T>G NP_001191232.1:p.Phe597Val
NM_201413.2:c.2011T>G NP_958816.1:p.Phe671Val
NM_201414.2:c.1843T>G NP_958817.1:p.Phe615Val
NM_000484.4:c.2068T>G MANE Select NP_000475.1:p.Phe690Val
NM_001136129.3:c.1675T>G NP_001129601.1:p.Phe559Val
NM_001136130.3:c.1900T>G NP_001129602.1:p.Phe634Val
NM_001204301.2:c.2014T>G NP_001191230.1:p.Phe672Val
NM_001204302.2:c.1957T>G NP_001191231.1:p.Phe653Val
NM_001204303.2:c.1789T>G NP_001191232.1:p.Phe597Val
NM_201413.3:c.2011T>G NP_958816.1:p.Phe671Val
NM_201414.3:c.1843T>G NP_958817.1:p.Phe615Val
NM_001136131.3:c.1738T>G NP_001129603.1:p.Phe580Val
NM_001385253.1:c.1900T>G NP_001372182.1:p.Phe634Val