Canonical Allele Identifier: CA409805688
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891855T>G , CM000683.2:g.25891855T>G GRCh38
NC_000021.8:g.27264167T>G , CM000683.1:g.27264167T>G GRCh37
NC_000021.7:g.26186038T>G NCBI36
NG_007376.1:g.283966A>C
NG_007376.2:g.284274A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2078A>C MANE Select ENSP00000284981.4:p.Glu693Ala
ENST00000346798.7:c.2078A>C ENSP00000284981.4:p.Glu693Ala
ENST00000348990.9:c.1853A>C ENSP00000345463.5:p.Glu618Ala
ENST00000354192.7:c.1685A>C ENSP00000346129.3:p.Glu562Ala
ENST00000357903.7:c.2021A>C ENSP00000350578.3:p.Glu674Ala
ENST00000358918.7:c.2024A>C ENSP00000351796.3:p.Glu675Ala
ENST00000359726.7:c.1748A>C ENSP00000352760.4:p.Glu583Ala
ENST00000439274.6:c.1910A>C ENSP00000398879.2:p.Glu637Ala
ENST00000440126.7:c.2006A>C ENSP00000387483.2:p.Glu669Ala
NM_000484.3:c.2078A>C NP_000475.1:p.Glu693Ala
NM_001136016.3:c.2006A>C NP_001129488.1:p.Glu669Ala
NM_001136129.2:c.1685A>C NP_001129601.1:p.Glu562Ala
NM_001136130.2:c.1910A>C NP_001129602.1:p.Glu637Ala
NM_001136131.2:c.1748A>C NP_001129603.1:p.Glu583Ala
NM_001204301.1:c.2024A>C NP_001191230.1:p.Glu675Ala
NM_001204302.1:c.1967A>C NP_001191231.1:p.Glu656Ala
NM_001204303.1:c.1799A>C NP_001191232.1:p.Glu600Ala
NM_201413.2:c.2021A>C NP_958816.1:p.Glu674Ala
NM_201414.2:c.1853A>C NP_958817.1:p.Glu618Ala
NM_000484.4:c.2078A>C MANE Select NP_000475.1:p.Glu693Ala
NM_001136129.3:c.1685A>C NP_001129601.1:p.Glu562Ala
NM_001136130.3:c.1910A>C NP_001129602.1:p.Glu637Ala
NM_001204301.2:c.2024A>C NP_001191230.1:p.Glu675Ala
NM_001204302.2:c.1967A>C NP_001191231.1:p.Glu656Ala
NM_001204303.2:c.1799A>C NP_001191232.1:p.Glu600Ala
NM_201413.3:c.2021A>C NP_958816.1:p.Glu674Ala
NM_201414.3:c.1853A>C NP_958817.1:p.Glu618Ala
NM_001136131.3:c.1748A>C NP_001129603.1:p.Glu583Ala
NM_001385253.1:c.1910A>C NP_001372182.1:p.Glu637Ala