Canonical Allele Identifier: CA409806590
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897671A>C , CM000683.2:g.25897671A>C GRCh38
NC_000021.8:g.27269983A>C , CM000683.1:g.27269983A>C GRCh37
NC_000021.7:g.26191854A>C NCBI36
NG_007376.1:g.278150T>G
NG_007376.2:g.278458T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1933T>G
ENST00000707133.1:n.363T>G
ENST00000707134.1:n.632T>G
ENST00000346798.8:c.1966T>G MANE Select ENSP00000284981.4:p.Ser656Ala
ENST00000346798.7:c.1966T>G ENSP00000284981.4:p.Ser656Ala
ENST00000348990.9:c.1741T>G ENSP00000345463.5:p.Ser581Ala
ENST00000354192.7:c.1573T>G ENSP00000346129.3:p.Ser525Ala
ENST00000357903.7:c.1909T>G ENSP00000350578.3:p.Ser637Ala
ENST00000358918.7:c.1912T>G ENSP00000351796.3:p.Ser638Ala
ENST00000359726.7:c.1636T>G ENSP00000352760.4:p.Ser546Ala
ENST00000439274.6:c.1798T>G ENSP00000398879.2:p.Ser600Ala
ENST00000440126.7:c.1894T>G ENSP00000387483.2:p.Ser632Ala
ENST00000464867.1:n.313T>G
NM_000484.3:c.1966T>G NP_000475.1:p.Ser656Ala
NM_001136016.3:c.1894T>G NP_001129488.1:p.Ser632Ala
NM_001136129.2:c.1573T>G NP_001129601.1:p.Ser525Ala
NM_001136130.2:c.1798T>G NP_001129602.1:p.Ser600Ala
NM_001136131.2:c.1636T>G NP_001129603.1:p.Ser546Ala
NM_001204301.1:c.1912T>G NP_001191230.1:p.Ser638Ala
NM_001204302.1:c.1855T>G NP_001191231.1:p.Ser619Ala
NM_001204303.1:c.1687T>G NP_001191232.1:p.Ser563Ala
NM_201413.2:c.1909T>G NP_958816.1:p.Ser637Ala
NM_201414.2:c.1741T>G NP_958817.1:p.Ser581Ala
NM_000484.4:c.1966T>G MANE Select NP_000475.1:p.Ser656Ala
NM_001136129.3:c.1573T>G NP_001129601.1:p.Ser525Ala
NM_001136130.3:c.1798T>G NP_001129602.1:p.Ser600Ala
NM_001204301.2:c.1912T>G NP_001191230.1:p.Ser638Ala
NM_001204302.2:c.1855T>G NP_001191231.1:p.Ser619Ala
NM_001204303.2:c.1687T>G NP_001191232.1:p.Ser563Ala
NM_201413.3:c.1909T>G NP_958816.1:p.Ser637Ala
NM_201414.3:c.1741T>G NP_958817.1:p.Ser581Ala
NM_001136131.3:c.1636T>G NP_001129603.1:p.Ser546Ala
NM_001385253.1:c.1798T>G NP_001372182.1:p.Ser600Ala