Canonical Allele Identifier: CA409805663
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891843G>T , CM000683.2:g.25891843G>T GRCh38
NC_000021.8:g.27264155G>T , CM000683.1:g.27264155G>T GRCh37
NC_000021.7:g.26186026G>T NCBI36
NG_007376.1:g.283978C>A
NG_007376.2:g.284286C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2057C>A
ENST00000707133.1:n.487C>A
ENST00000707134.1:n.756C>A
ENST00000346798.8:c.2090C>A MANE Select ENSP00000284981.4:p.Ser697Ter
ENST00000346798.7:c.2090C>A ENSP00000284981.4:p.Ser697Ter
ENST00000348990.9:c.1865C>A ENSP00000345463.5:p.Ser622Ter
ENST00000354192.7:c.1697C>A ENSP00000346129.3:p.Ser566Ter
ENST00000357903.7:c.2033C>A ENSP00000350578.3:p.Ser678Ter
ENST00000358918.7:c.2036C>A ENSP00000351796.3:p.Ser679Ter
ENST00000359726.7:c.1760C>A ENSP00000352760.4:p.Ser587Ter
ENST00000439274.6:c.1922C>A ENSP00000398879.2:p.Ser641Ter
ENST00000440126.7:c.2018C>A ENSP00000387483.2:p.Ser673Ter
ENST00000464867.1:n.437C>A
NM_000484.3:c.2090C>A NP_000475.1:p.Ser697Ter
NM_001136016.3:c.2018C>A NP_001129488.1:p.Ser673Ter
NM_001136129.2:c.1697C>A NP_001129601.1:p.Ser566Ter
NM_001136130.2:c.1922C>A NP_001129602.1:p.Ser641Ter
NM_001136131.2:c.1760C>A NP_001129603.1:p.Ser587Ter
NM_001204301.1:c.2036C>A NP_001191230.1:p.Ser679Ter
NM_001204302.1:c.1979C>A NP_001191231.1:p.Ser660Ter
NM_001204303.1:c.1811C>A NP_001191232.1:p.Ser604Ter
NM_201413.2:c.2033C>A NP_958816.1:p.Ser678Ter
NM_201414.2:c.1865C>A NP_958817.1:p.Ser622Ter
NM_000484.4:c.2090C>A MANE Select NP_000475.1:p.Ser697Ter
NM_001136129.3:c.1697C>A NP_001129601.1:p.Ser566Ter
NM_001136130.3:c.1922C>A NP_001129602.1:p.Ser641Ter
NM_001204301.2:c.2036C>A NP_001191230.1:p.Ser679Ter
NM_001204302.2:c.1979C>A NP_001191231.1:p.Ser660Ter
NM_001204303.2:c.1811C>A NP_001191232.1:p.Ser604Ter
NM_201413.3:c.2033C>A NP_958816.1:p.Ser678Ter
NM_201414.3:c.1865C>A NP_958817.1:p.Ser622Ter
NM_001136131.3:c.1760C>A NP_001129603.1:p.Ser587Ter
NM_001385253.1:c.1922C>A NP_001372182.1:p.Ser641Ter