Canonical Allele Identifier: CA409806592
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1933T>A
ENST00000707133.1:n.363T>A
ENST00000707134.1:n.632T>A
ENST00000346798.8:c.1966T>A MANE Select ENSP00000284981.4:p.Ser656Thr
ENST00000346798.7:c.1966T>A ENSP00000284981.4:p.Ser656Thr
ENST00000348990.9:c.1741T>A ENSP00000345463.5:p.Ser581Thr
ENST00000354192.7:c.1573T>A ENSP00000346129.3:p.Ser525Thr
ENST00000357903.7:c.1909T>A ENSP00000350578.3:p.Ser637Thr
ENST00000358918.7:c.1912T>A ENSP00000351796.3:p.Ser638Thr
ENST00000359726.7:c.1636T>A ENSP00000352760.4:p.Ser546Thr
ENST00000439274.6:c.1798T>A ENSP00000398879.2:p.Ser600Thr
ENST00000440126.7:c.1894T>A ENSP00000387483.2:p.Ser632Thr
ENST00000464867.1:n.313T>A
NM_000484.3:c.1966T>A NP_000475.1:p.Ser656Thr
NM_001136016.3:c.1894T>A NP_001129488.1:p.Ser632Thr
NM_001136129.2:c.1573T>A NP_001129601.1:p.Ser525Thr
NM_001136130.2:c.1798T>A NP_001129602.1:p.Ser600Thr
NM_001136131.2:c.1636T>A NP_001129603.1:p.Ser546Thr
NM_001204301.1:c.1912T>A NP_001191230.1:p.Ser638Thr
NM_001204302.1:c.1855T>A NP_001191231.1:p.Ser619Thr
NM_001204303.1:c.1687T>A NP_001191232.1:p.Ser563Thr
NM_201413.2:c.1909T>A NP_958816.1:p.Ser637Thr
NM_201414.2:c.1741T>A NP_958817.1:p.Ser581Thr
NM_000484.4:c.1966T>A MANE Select NP_000475.1:p.Ser656Thr
NM_001136129.3:c.1573T>A NP_001129601.1:p.Ser525Thr
NM_001136130.3:c.1798T>A NP_001129602.1:p.Ser600Thr
NM_001204301.2:c.1912T>A NP_001191230.1:p.Ser638Thr
NM_001204302.2:c.1855T>A NP_001191231.1:p.Ser619Thr
NM_001204303.2:c.1687T>A NP_001191232.1:p.Ser563Thr
NM_201413.3:c.1909T>A NP_958816.1:p.Ser637Thr
NM_201414.3:c.1741T>A NP_958817.1:p.Ser581Thr
NM_001136131.3:c.1636T>A NP_001129603.1:p.Ser546Thr
NM_001385253.1:c.1798T>A NP_001372182.1:p.Ser600Thr