Canonical Allele Identifier: CA409805661
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2057C>T
ENST00000707133.1:n.487C>T
ENST00000707134.1:n.756C>T
ENST00000346798.8:c.2090C>T MANE Select ENSP00000284981.4:p.Ser697Leu
ENST00000346798.7:c.2090C>T ENSP00000284981.4:p.Ser697Leu
ENST00000348990.9:c.1865C>T ENSP00000345463.5:p.Ser622Leu
ENST00000354192.7:c.1697C>T ENSP00000346129.3:p.Ser566Leu
ENST00000357903.7:c.2033C>T ENSP00000350578.3:p.Ser678Leu
ENST00000358918.7:c.2036C>T ENSP00000351796.3:p.Ser679Leu
ENST00000359726.7:c.1760C>T ENSP00000352760.4:p.Ser587Leu
ENST00000439274.6:c.1922C>T ENSP00000398879.2:p.Ser641Leu
ENST00000440126.7:c.2018C>T ENSP00000387483.2:p.Ser673Leu
ENST00000464867.1:n.437C>T
NM_000484.3:c.2090C>T NP_000475.1:p.Ser697Leu
NM_001136016.3:c.2018C>T NP_001129488.1:p.Ser673Leu
NM_001136129.2:c.1697C>T NP_001129601.1:p.Ser566Leu
NM_001136130.2:c.1922C>T NP_001129602.1:p.Ser641Leu
NM_001136131.2:c.1760C>T NP_001129603.1:p.Ser587Leu
NM_001204301.1:c.2036C>T NP_001191230.1:p.Ser679Leu
NM_001204302.1:c.1979C>T NP_001191231.1:p.Ser660Leu
NM_001204303.1:c.1811C>T NP_001191232.1:p.Ser604Leu
NM_201413.2:c.2033C>T NP_958816.1:p.Ser678Leu
NM_201414.2:c.1865C>T NP_958817.1:p.Ser622Leu
NM_000484.4:c.2090C>T MANE Select NP_000475.1:p.Ser697Leu
NM_001136129.3:c.1697C>T NP_001129601.1:p.Ser566Leu
NM_001136130.3:c.1922C>T NP_001129602.1:p.Ser641Leu
NM_001204301.2:c.2036C>T NP_001191230.1:p.Ser679Leu
NM_001204302.2:c.1979C>T NP_001191231.1:p.Ser660Leu
NM_001204303.2:c.1811C>T NP_001191232.1:p.Ser604Leu
NM_201413.3:c.2033C>T NP_958816.1:p.Ser678Leu
NM_201414.3:c.1865C>T NP_958817.1:p.Ser622Leu
NM_001136131.3:c.1760C>T NP_001129603.1:p.Ser587Leu
NM_001385253.1:c.1922C>T NP_001372182.1:p.Ser641Leu