Canonical Allele Identifier: CA409805476
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2150A>G
ENST00000707133.1:n.580A>G
ENST00000707134.1:n.849A>G
ENST00000346798.8:c.2183A>G MANE Select ENSP00000284981.4:p.Tyr728Cys
ENST00000346798.7:c.2183A>G ENSP00000284981.4:p.Tyr728Cys
ENST00000348990.9:c.1958A>G ENSP00000345463.5:p.Tyr653Cys
ENST00000354192.7:c.1790A>G ENSP00000346129.3:p.Tyr597Cys
ENST00000357903.7:c.2126A>G ENSP00000350578.3:p.Tyr709Cys
ENST00000358918.7:c.2129A>G ENSP00000351796.3:p.Tyr710Cys
ENST00000359726.7:c.1853A>G ENSP00000352760.4:p.Tyr618Cys
ENST00000439274.6:c.2015A>G ENSP00000398879.2:p.Tyr672Cys
ENST00000440126.7:c.2111A>G ENSP00000387483.2:p.Tyr704Cys
ENST00000464867.1:n.530A>G
NM_000484.3:c.2183A>G NP_000475.1:p.Tyr728Cys
NM_001136016.3:c.2111A>G NP_001129488.1:p.Tyr704Cys
NM_001136129.2:c.1790A>G NP_001129601.1:p.Tyr597Cys
NM_001136130.2:c.2015A>G NP_001129602.1:p.Tyr672Cys
NM_001136131.2:c.1853A>G NP_001129603.1:p.Tyr618Cys
NM_001204301.1:c.2129A>G NP_001191230.1:p.Tyr710Cys
NM_001204302.1:c.2072A>G NP_001191231.1:p.Tyr691Cys
NM_001204303.1:c.1904A>G NP_001191232.1:p.Tyr635Cys
NM_201413.2:c.2126A>G NP_958816.1:p.Tyr709Cys
NM_201414.2:c.1958A>G NP_958817.1:p.Tyr653Cys
NM_000484.4:c.2183A>G MANE Select NP_000475.1:p.Tyr728Cys
NM_001136129.3:c.1790A>G NP_001129601.1:p.Tyr597Cys
NM_001136130.3:c.2015A>G NP_001129602.1:p.Tyr672Cys
NM_001204301.2:c.2129A>G NP_001191230.1:p.Tyr710Cys
NM_001204302.2:c.2072A>G NP_001191231.1:p.Tyr691Cys
NM_001204303.2:c.1904A>G NP_001191232.1:p.Tyr635Cys
NM_201413.3:c.2126A>G NP_958816.1:p.Tyr709Cys
NM_201414.3:c.1958A>G NP_958817.1:p.Tyr653Cys
NM_001136131.3:c.1853A>G NP_001129603.1:p.Tyr618Cys
NM_001385253.1:c.2015A>G NP_001372182.1:p.Tyr672Cys