Canonical Allele Identifier: CA409805700
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891862A>C , CM000683.2:g.25891862A>C GRCh38
NC_000021.8:g.27264174A>C , CM000683.1:g.27264174A>C GRCh37
NC_000021.7:g.26186045A>C NCBI36
NG_007376.1:g.283959T>G
NG_007376.2:g.284267T>G

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2071T>G NP_000475.1:p.Phe691Val
NM_001136016.3:c.1999T>G NP_001129488.1:p.Phe667Val
NM_001136129.2:c.1678T>G NP_001129601.1:p.Phe560Val
NM_001136130.2:c.1903T>G NP_001129602.1:p.Phe635Val
NM_001136131.2:c.1741T>G NP_001129603.1:p.Phe581Val
NM_001204301.1:c.2017T>G NP_001191230.1:p.Phe673Val
NM_001204302.1:c.1960T>G NP_001191231.1:p.Phe654Val
NM_001204303.1:c.1792T>G NP_001191232.1:p.Phe598Val
NM_201413.2:c.2014T>G NP_958816.1:p.Phe672Val
NM_201414.2:c.1846T>G NP_958817.1:p.Phe616Val
NM_000484.4:c.2071T>G MANE Select NP_000475.1:p.Phe691Val
NM_001136129.3:c.1678T>G NP_001129601.1:p.Phe560Val
NM_001136130.3:c.1903T>G NP_001129602.1:p.Phe635Val
NM_001204301.2:c.2017T>G NP_001191230.1:p.Phe673Val
NM_001204302.2:c.1960T>G NP_001191231.1:p.Phe654Val
NM_001204303.2:c.1792T>G NP_001191232.1:p.Phe598Val
NM_201413.3:c.2014T>G NP_958816.1:p.Phe672Val
NM_201414.3:c.1846T>G NP_958817.1:p.Phe616Val
NM_001136131.3:c.1741T>G NP_001129603.1:p.Phe581Val
NM_001385253.1:c.1903T>G NP_001372182.1:p.Phe635Val
ENST00000346798.7:c.2071T>G ENSP00000284981.4:p.Phe691Val
ENST00000348990.9:c.1846T>G ENSP00000345463.5:p.Phe616Val
ENST00000354192.7:c.1678T>G ENSP00000346129.3:p.Phe560Val
ENST00000357903.7:c.2014T>G ENSP00000350578.3:p.Phe672Val
ENST00000358918.7:c.2017T>G ENSP00000351796.3:p.Phe673Val
ENST00000359726.7:c.1741T>G ENSP00000352760.4:p.Phe581Val
ENST00000439274.6:c.1903T>G ENSP00000398879.2:p.Phe635Val
ENST00000440126.7:c.1999T>G ENSP00000387483.2:p.Phe667Val
ENST00000464867.1:n.418T>G