Canonical Allele Identifier: CA409805686
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891854T>G , CM000683.2:g.25891854T>G GRCh38
NC_000021.8:g.27264166T>G , CM000683.1:g.27264166T>G GRCh37
NC_000021.7:g.26186037T>G NCBI36
NG_007376.1:g.283967A>C
NG_007376.2:g.284275A>C

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2079A>C NP_000475.1:p.Glu693Asp
NM_001136016.3:c.2007A>C NP_001129488.1:p.Glu669Asp
NM_001136129.2:c.1686A>C NP_001129601.1:p.Glu562Asp
NM_001136130.2:c.1911A>C NP_001129602.1:p.Glu637Asp
NM_001136131.2:c.1749A>C NP_001129603.1:p.Glu583Asp
NM_001204301.1:c.2025A>C NP_001191230.1:p.Glu675Asp
NM_001204302.1:c.1968A>C NP_001191231.1:p.Glu656Asp
NM_001204303.1:c.1800A>C NP_001191232.1:p.Glu600Asp
NM_201413.2:c.2022A>C NP_958816.1:p.Glu674Asp
NM_201414.2:c.1854A>C NP_958817.1:p.Glu618Asp
NM_000484.4:c.2079A>C MANE Select NP_000475.1:p.Glu693Asp
NM_001136129.3:c.1686A>C NP_001129601.1:p.Glu562Asp
NM_001136130.3:c.1911A>C NP_001129602.1:p.Glu637Asp
NM_001204301.2:c.2025A>C NP_001191230.1:p.Glu675Asp
NM_001204302.2:c.1968A>C NP_001191231.1:p.Glu656Asp
NM_001204303.2:c.1800A>C NP_001191232.1:p.Glu600Asp
NM_201413.3:c.2022A>C NP_958816.1:p.Glu674Asp
NM_201414.3:c.1854A>C NP_958817.1:p.Glu618Asp
NM_001136131.3:c.1749A>C NP_001129603.1:p.Glu583Asp
NM_001385253.1:c.1911A>C NP_001372182.1:p.Glu637Asp
ENST00000346798.7:c.2079A>C ENSP00000284981.4:p.Glu693Asp
ENST00000348990.9:c.1854A>C ENSP00000345463.5:p.Glu618Asp
ENST00000354192.7:c.1686A>C ENSP00000346129.3:p.Glu562Asp
ENST00000357903.7:c.2022A>C ENSP00000350578.3:p.Glu674Asp
ENST00000358918.7:c.2025A>C ENSP00000351796.3:p.Glu675Asp
ENST00000359726.7:c.1749A>C ENSP00000352760.4:p.Glu583Asp
ENST00000439274.6:c.1911A>C ENSP00000398879.2:p.Glu637Asp
ENST00000440126.7:c.2007A>C ENSP00000387483.2:p.Glu669Asp
ENST00000464867.1:n.426A>C