Canonical Allele Identifier: CA2383551645
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891856C= , CM000683.2:g.25891856C= GRCh38
NC_000021.8:g.27264168C= , CM000683.1:g.27264168C= GRCh37
NC_000021.7:g.26186039C= NCBI36
NG_007376.1:g.283965G=
NG_007376.2:g.284273G=

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2044G=
ENST00000707133.1:n.474G=
ENST00000707134.1:n.743G=
ENST00000346798.8:c.2077G= MANE Select ENSP00000284981.4:p.Glu693=
ENST00000346798.7:c.2077G= ENSP00000284981.4:p.Glu693=
ENST00000348990.9:c.1852G= ENSP00000345463.5:p.Glu618=
ENST00000354192.7:c.1684G= ENSP00000346129.3:p.Glu562=
ENST00000357903.7:c.2020G= ENSP00000350578.3:p.Glu674=
ENST00000358918.7:c.2023G= ENSP00000351796.3:p.Glu675=
ENST00000359726.7:c.1747G= ENSP00000352760.4:p.Glu583=
ENST00000439274.6:c.1909G= ENSP00000398879.2:p.Glu637=
ENST00000440126.7:c.2005G= ENSP00000387483.2:p.Glu669=
ENST00000464867.1:n.424G=
NM_000484.3:c.2077G= NP_000475.1:p.Glu693=
NM_001136016.3:c.2005G= NP_001129488.1:p.Glu669=
NM_001136129.2:c.1684G= NP_001129601.1:p.Glu562=
NM_001136130.2:c.1909G= NP_001129602.1:p.Glu637=
NM_001136131.2:c.1747G= NP_001129603.1:p.Glu583=
NM_001204301.1:c.2023G= NP_001191230.1:p.Glu675=
NM_001204302.1:c.1966G= NP_001191231.1:p.Glu656=
NM_001204303.1:c.1798G= NP_001191232.1:p.Glu600=
NM_201413.2:c.2020G= NP_958816.1:p.Glu674=
NM_201414.2:c.1852G= NP_958817.1:p.Glu618=
NM_000484.4:c.2077G= MANE Select NP_000475.1:p.Glu693=
NM_001136129.3:c.1684G= NP_001129601.1:p.Glu562=
NM_001136130.3:c.1909G= NP_001129602.1:p.Glu637=
NM_001204301.2:c.2023G= NP_001191230.1:p.Glu675=
NM_001204302.2:c.1966G= NP_001191231.1:p.Glu656=
NM_001204303.2:c.1798G= NP_001191232.1:p.Glu600=
NM_201413.3:c.2020G= NP_958816.1:p.Glu674=
NM_201414.3:c.1852G= NP_958817.1:p.Glu618=
NM_001136131.3:c.1747G= NP_001129603.1:p.Glu583=
NM_001385253.1:c.1909G= NP_001372182.1:p.Glu637=