Canonical Allele Identifier: CA409805704
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891864A>C , CM000683.2:g.25891864A>C GRCh38
NC_000021.8:g.27264176A>C , CM000683.1:g.27264176A>C GRCh37
NC_000021.7:g.26186047A>C NCBI36
NG_007376.1:g.283957T>G
NG_007376.2:g.284265T>G

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2069T>G NP_000475.1:p.Phe690Cys
NM_001136016.3:c.1997T>G NP_001129488.1:p.Phe666Cys
NM_001136129.2:c.1676T>G NP_001129601.1:p.Phe559Cys
NM_001136130.2:c.1901T>G NP_001129602.1:p.Phe634Cys
NM_001136131.2:c.1739T>G NP_001129603.1:p.Phe580Cys
NM_001204301.1:c.2015T>G NP_001191230.1:p.Phe672Cys
NM_001204302.1:c.1958T>G NP_001191231.1:p.Phe653Cys
NM_001204303.1:c.1790T>G NP_001191232.1:p.Phe597Cys
NM_201413.2:c.2012T>G NP_958816.1:p.Phe671Cys
NM_201414.2:c.1844T>G NP_958817.1:p.Phe615Cys
NM_000484.4:c.2069T>G MANE Select NP_000475.1:p.Phe690Cys
NM_001136129.3:c.1676T>G NP_001129601.1:p.Phe559Cys
NM_001136130.3:c.1901T>G NP_001129602.1:p.Phe634Cys
NM_001204301.2:c.2015T>G NP_001191230.1:p.Phe672Cys
NM_001204302.2:c.1958T>G NP_001191231.1:p.Phe653Cys
NM_001204303.2:c.1790T>G NP_001191232.1:p.Phe597Cys
NM_201413.3:c.2012T>G NP_958816.1:p.Phe671Cys
NM_201414.3:c.1844T>G NP_958817.1:p.Phe615Cys
NM_001136131.3:c.1739T>G NP_001129603.1:p.Phe580Cys
NM_001385253.1:c.1901T>G NP_001372182.1:p.Phe634Cys
ENST00000346798.7:c.2069T>G ENSP00000284981.4:p.Phe690Cys
ENST00000348990.9:c.1844T>G ENSP00000345463.5:p.Phe615Cys
ENST00000354192.7:c.1676T>G ENSP00000346129.3:p.Phe559Cys
ENST00000357903.7:c.2012T>G ENSP00000350578.3:p.Phe671Cys
ENST00000358918.7:c.2015T>G ENSP00000351796.3:p.Phe672Cys
ENST00000359726.7:c.1739T>G ENSP00000352760.4:p.Phe580Cys
ENST00000439274.6:c.1901T>G ENSP00000398879.2:p.Phe634Cys
ENST00000440126.7:c.1997T>G ENSP00000387483.2:p.Phe666Cys
ENST00000464867.1:n.416T>G