Canonical Allele Identifier: CA409806591
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1933T>C
ENST00000707133.1:n.363T>C
ENST00000707134.1:n.632T>C
ENST00000346798.8:c.1966T>C MANE Select ENSP00000284981.4:p.Ser656Pro
ENST00000346798.7:c.1966T>C ENSP00000284981.4:p.Ser656Pro
ENST00000348990.9:c.1741T>C ENSP00000345463.5:p.Ser581Pro
ENST00000354192.7:c.1573T>C ENSP00000346129.3:p.Ser525Pro
ENST00000357903.7:c.1909T>C ENSP00000350578.3:p.Ser637Pro
ENST00000358918.7:c.1912T>C ENSP00000351796.3:p.Ser638Pro
ENST00000359726.7:c.1636T>C ENSP00000352760.4:p.Ser546Pro
ENST00000439274.6:c.1798T>C ENSP00000398879.2:p.Ser600Pro
ENST00000440126.7:c.1894T>C ENSP00000387483.2:p.Ser632Pro
ENST00000464867.1:n.313T>C
NM_000484.3:c.1966T>C NP_000475.1:p.Ser656Pro
NM_001136016.3:c.1894T>C NP_001129488.1:p.Ser632Pro
NM_001136129.2:c.1573T>C NP_001129601.1:p.Ser525Pro
NM_001136130.2:c.1798T>C NP_001129602.1:p.Ser600Pro
NM_001136131.2:c.1636T>C NP_001129603.1:p.Ser546Pro
NM_001204301.1:c.1912T>C NP_001191230.1:p.Ser638Pro
NM_001204302.1:c.1855T>C NP_001191231.1:p.Ser619Pro
NM_001204303.1:c.1687T>C NP_001191232.1:p.Ser563Pro
NM_201413.2:c.1909T>C NP_958816.1:p.Ser637Pro
NM_201414.2:c.1741T>C NP_958817.1:p.Ser581Pro
NM_000484.4:c.1966T>C MANE Select NP_000475.1:p.Ser656Pro
NM_001136129.3:c.1573T>C NP_001129601.1:p.Ser525Pro
NM_001136130.3:c.1798T>C NP_001129602.1:p.Ser600Pro
NM_001204301.2:c.1912T>C NP_001191230.1:p.Ser638Pro
NM_001204302.2:c.1855T>C NP_001191231.1:p.Ser619Pro
NM_001204303.2:c.1687T>C NP_001191232.1:p.Ser563Pro
NM_201413.3:c.1909T>C NP_958816.1:p.Ser637Pro
NM_201414.3:c.1741T>C NP_958817.1:p.Ser581Pro
NM_001136131.3:c.1636T>C NP_001129603.1:p.Ser546Pro
NM_001385253.1:c.1798T>C NP_001372182.1:p.Ser600Pro