Canonical Allele Identifier: CA409805439
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs1555889054

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891735T>G , CM000683.2:g.25891735T>G GRCh38
NC_000021.8:g.27264047T>G , CM000683.1:g.27264047T>G GRCh37
NC_000021.7:g.26185918T>G NCBI36
NG_007376.1:g.284086A>C
NG_007376.2:g.284394A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2165A>C
ENST00000707133.1:n.595A>C
ENST00000707134.1:n.864A>C
ENST00000346798.8:c.2198A>C MANE Select ENSP00000284981.4:p.His733Pro
ENST00000346798.7:c.2198A>C ENSP00000284981.4:p.His733Pro
ENST00000348990.9:c.1973A>C ENSP00000345463.5:p.His658Pro
ENST00000354192.7:c.1805A>C ENSP00000346129.3:p.His602Pro
ENST00000357903.7:c.2141A>C ENSP00000350578.3:p.His714Pro
ENST00000358918.7:c.2144A>C ENSP00000351796.3:p.His715Pro
ENST00000359726.7:c.1868A>C ENSP00000352760.4:p.His623Pro
ENST00000439274.6:c.2030A>C ENSP00000398879.2:p.His677Pro
ENST00000440126.7:c.2126A>C ENSP00000387483.2:p.His709Pro
ENST00000464867.1:n.545A>C
NM_000484.3:c.2198A>C NP_000475.1:p.His733Pro
NM_001136016.3:c.2126A>C NP_001129488.1:p.His709Pro
NM_001136129.2:c.1805A>C NP_001129601.1:p.His602Pro
NM_001136130.2:c.2030A>C NP_001129602.1:p.His677Pro
NM_001136131.2:c.1868A>C NP_001129603.1:p.His623Pro
NM_001204301.1:c.2144A>C NP_001191230.1:p.His715Pro
NM_001204302.1:c.2087A>C NP_001191231.1:p.His696Pro
NM_001204303.1:c.1919A>C NP_001191232.1:p.His640Pro
NM_201413.2:c.2141A>C NP_958816.1:p.His714Pro
NM_201414.2:c.1973A>C NP_958817.1:p.His658Pro
NM_000484.4:c.2198A>C MANE Select NP_000475.1:p.His733Pro
NM_001136129.3:c.1805A>C NP_001129601.1:p.His602Pro
NM_001136130.3:c.2030A>C NP_001129602.1:p.His677Pro
NM_001204301.2:c.2144A>C NP_001191230.1:p.His715Pro
NM_001204302.2:c.2087A>C NP_001191231.1:p.His696Pro
NM_001204303.2:c.1919A>C NP_001191232.1:p.His640Pro
NM_201413.3:c.2141A>C NP_958816.1:p.His714Pro
NM_201414.3:c.1973A>C NP_958817.1:p.His658Pro
NM_001136131.3:c.1868A>C NP_001129603.1:p.His623Pro
NM_001385253.1:c.2030A>C NP_001372182.1:p.His677Pro