Canonical Allele Identifier: CA409805474
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891750T>A , CM000683.2:g.25891750T>A GRCh38
NC_000021.8:g.27264062T>A , CM000683.1:g.27264062T>A GRCh37
NC_000021.7:g.26185933T>A NCBI36
NG_007376.1:g.284071A>T
NG_007376.2:g.284379A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2150A>T
ENST00000707133.1:n.580A>T
ENST00000707134.1:n.849A>T
ENST00000346798.8:c.2183A>T MANE Select ENSP00000284981.4:p.Tyr728Phe
ENST00000346798.7:c.2183A>T ENSP00000284981.4:p.Tyr728Phe
ENST00000348990.9:c.1958A>T ENSP00000345463.5:p.Tyr653Phe
ENST00000354192.7:c.1790A>T ENSP00000346129.3:p.Tyr597Phe
ENST00000357903.7:c.2126A>T ENSP00000350578.3:p.Tyr709Phe
ENST00000358918.7:c.2129A>T ENSP00000351796.3:p.Tyr710Phe
ENST00000359726.7:c.1853A>T ENSP00000352760.4:p.Tyr618Phe
ENST00000439274.6:c.2015A>T ENSP00000398879.2:p.Tyr672Phe
ENST00000440126.7:c.2111A>T ENSP00000387483.2:p.Tyr704Phe
ENST00000464867.1:n.530A>T
NM_000484.3:c.2183A>T NP_000475.1:p.Tyr728Phe
NM_001136016.3:c.2111A>T NP_001129488.1:p.Tyr704Phe
NM_001136129.2:c.1790A>T NP_001129601.1:p.Tyr597Phe
NM_001136130.2:c.2015A>T NP_001129602.1:p.Tyr672Phe
NM_001136131.2:c.1853A>T NP_001129603.1:p.Tyr618Phe
NM_001204301.1:c.2129A>T NP_001191230.1:p.Tyr710Phe
NM_001204302.1:c.2072A>T NP_001191231.1:p.Tyr691Phe
NM_001204303.1:c.1904A>T NP_001191232.1:p.Tyr635Phe
NM_201413.2:c.2126A>T NP_958816.1:p.Tyr709Phe
NM_201414.2:c.1958A>T NP_958817.1:p.Tyr653Phe
NM_000484.4:c.2183A>T MANE Select NP_000475.1:p.Tyr728Phe
NM_001136129.3:c.1790A>T NP_001129601.1:p.Tyr597Phe
NM_001136130.3:c.2015A>T NP_001129602.1:p.Tyr672Phe
NM_001204301.2:c.2129A>T NP_001191230.1:p.Tyr710Phe
NM_001204302.2:c.2072A>T NP_001191231.1:p.Tyr691Phe
NM_001204303.2:c.1904A>T NP_001191232.1:p.Tyr635Phe
NM_201413.3:c.2126A>T NP_958816.1:p.Tyr709Phe
NM_201414.3:c.1958A>T NP_958817.1:p.Tyr653Phe
NM_001136131.3:c.1853A>T NP_001129603.1:p.Tyr618Phe
NM_001385253.1:c.2015A>T NP_001372182.1:p.Tyr672Phe