Canonical Allele Identifier: CA409805498
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891759T>A , CM000683.2:g.25891759T>A GRCh38
NC_000021.8:g.27264071T>A , CM000683.1:g.27264071T>A GRCh37
NC_000021.7:g.26185942T>A NCBI36
NG_007376.1:g.284062A>T
NG_007376.2:g.284370A>T

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2174A>T NP_000475.1:p.Lys725Met
NM_001136016.3:c.2102A>T NP_001129488.1:p.Lys701Met
NM_001136129.2:c.1781A>T NP_001129601.1:p.Lys594Met
NM_001136130.2:c.2006A>T NP_001129602.1:p.Lys669Met
NM_001136131.2:c.1844A>T NP_001129603.1:p.Lys615Met
NM_001204301.1:c.2120A>T NP_001191230.1:p.Lys707Met
NM_001204302.1:c.2063A>T NP_001191231.1:p.Lys688Met
NM_001204303.1:c.1895A>T NP_001191232.1:p.Lys632Met
NM_201413.2:c.2117A>T NP_958816.1:p.Lys706Met
NM_201414.2:c.1949A>T NP_958817.1:p.Lys650Met
NM_000484.4:c.2174A>T MANE Select NP_000475.1:p.Lys725Met
NM_001136129.3:c.1781A>T NP_001129601.1:p.Lys594Met
NM_001136130.3:c.2006A>T NP_001129602.1:p.Lys669Met
NM_001204301.2:c.2120A>T NP_001191230.1:p.Lys707Met
NM_001204302.2:c.2063A>T NP_001191231.1:p.Lys688Met
NM_001204303.2:c.1895A>T NP_001191232.1:p.Lys632Met
NM_201413.3:c.2117A>T NP_958816.1:p.Lys706Met
NM_201414.3:c.1949A>T NP_958817.1:p.Lys650Met
NM_001136131.3:c.1844A>T NP_001129603.1:p.Lys615Met
NM_001385253.1:c.2006A>T NP_001372182.1:p.Lys669Met
ENST00000346798.7:c.2174A>T ENSP00000284981.4:p.Lys725Met
ENST00000348990.9:c.1949A>T ENSP00000345463.5:p.Lys650Met
ENST00000354192.7:c.1781A>T ENSP00000346129.3:p.Lys594Met
ENST00000357903.7:c.2117A>T ENSP00000350578.3:p.Lys706Met
ENST00000358918.7:c.2120A>T ENSP00000351796.3:p.Lys707Met
ENST00000359726.7:c.1844A>T ENSP00000352760.4:p.Lys615Met
ENST00000439274.6:c.2006A>T ENSP00000398879.2:p.Lys669Met
ENST00000440126.7:c.2102A>T ENSP00000387483.2:p.Lys701Met
ENST00000464867.1:n.521A>T