Canonical Allele Identifier: CA409805664
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891844A>T , CM000683.2:g.25891844A>T GRCh38
NC_000021.8:g.27264156A>T , CM000683.1:g.27264156A>T GRCh37
NC_000021.7:g.26186027A>T NCBI36
NG_007376.1:g.283977T>A
NG_007376.2:g.284285T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2056T>A
ENST00000707133.1:n.486T>A
ENST00000707134.1:n.755T>A
ENST00000346798.8:c.2089T>A MANE Select ENSP00000284981.4:p.Ser697Thr
ENST00000346798.7:c.2089T>A ENSP00000284981.4:p.Ser697Thr
ENST00000348990.9:c.1864T>A ENSP00000345463.5:p.Ser622Thr
ENST00000354192.7:c.1696T>A ENSP00000346129.3:p.Ser566Thr
ENST00000357903.7:c.2032T>A ENSP00000350578.3:p.Ser678Thr
ENST00000358918.7:c.2035T>A ENSP00000351796.3:p.Ser679Thr
ENST00000359726.7:c.1759T>A ENSP00000352760.4:p.Ser587Thr
ENST00000439274.6:c.1921T>A ENSP00000398879.2:p.Ser641Thr
ENST00000440126.7:c.2017T>A ENSP00000387483.2:p.Ser673Thr
ENST00000464867.1:n.436T>A
NM_000484.3:c.2089T>A NP_000475.1:p.Ser697Thr
NM_001136016.3:c.2017T>A NP_001129488.1:p.Ser673Thr
NM_001136129.2:c.1696T>A NP_001129601.1:p.Ser566Thr
NM_001136130.2:c.1921T>A NP_001129602.1:p.Ser641Thr
NM_001136131.2:c.1759T>A NP_001129603.1:p.Ser587Thr
NM_001204301.1:c.2035T>A NP_001191230.1:p.Ser679Thr
NM_001204302.1:c.1978T>A NP_001191231.1:p.Ser660Thr
NM_001204303.1:c.1810T>A NP_001191232.1:p.Ser604Thr
NM_201413.2:c.2032T>A NP_958816.1:p.Ser678Thr
NM_201414.2:c.1864T>A NP_958817.1:p.Ser622Thr
NM_000484.4:c.2089T>A MANE Select NP_000475.1:p.Ser697Thr
NM_001136129.3:c.1696T>A NP_001129601.1:p.Ser566Thr
NM_001136130.3:c.1921T>A NP_001129602.1:p.Ser641Thr
NM_001204301.2:c.2035T>A NP_001191230.1:p.Ser679Thr
NM_001204302.2:c.1978T>A NP_001191231.1:p.Ser660Thr
NM_001204303.2:c.1810T>A NP_001191232.1:p.Ser604Thr
NM_201413.3:c.2032T>A NP_958816.1:p.Ser678Thr
NM_201414.3:c.1864T>A NP_958817.1:p.Ser622Thr
NM_001136131.3:c.1759T>A NP_001129603.1:p.Ser587Thr
NM_001385253.1:c.1921T>A NP_001372182.1:p.Ser641Thr