Canonical Allele Identifier: CA409805441
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2198A>G MANE Select ENSP00000284981.4:p.His733Arg
ENST00000346798.7:c.2198A>G ENSP00000284981.4:p.His733Arg
ENST00000348990.9:c.1973A>G ENSP00000345463.5:p.His658Arg
ENST00000354192.7:c.1805A>G ENSP00000346129.3:p.His602Arg
ENST00000357903.7:c.2141A>G ENSP00000350578.3:p.His714Arg
ENST00000358918.7:c.2144A>G ENSP00000351796.3:p.His715Arg
ENST00000359726.7:c.1868A>G ENSP00000352760.4:p.His623Arg
ENST00000439274.6:c.2030A>G ENSP00000398879.2:p.His677Arg
ENST00000440126.7:c.2126A>G ENSP00000387483.2:p.His709Arg
ENST00000464867.1:n.545A>G
NM_000484.3:c.2198A>G NP_000475.1:p.His733Arg
NM_001136016.3:c.2126A>G NP_001129488.1:p.His709Arg
NM_001136129.2:c.1805A>G NP_001129601.1:p.His602Arg
NM_001136130.2:c.2030A>G NP_001129602.1:p.His677Arg
NM_001136131.2:c.1868A>G NP_001129603.1:p.His623Arg
NM_001204301.1:c.2144A>G NP_001191230.1:p.His715Arg
NM_001204302.1:c.2087A>G NP_001191231.1:p.His696Arg
NM_001204303.1:c.1919A>G NP_001191232.1:p.His640Arg
NM_201413.2:c.2141A>G NP_958816.1:p.His714Arg
NM_201414.2:c.1973A>G NP_958817.1:p.His658Arg
NM_000484.4:c.2198A>G MANE Select NP_000475.1:p.His733Arg
NM_001136129.3:c.1805A>G NP_001129601.1:p.His602Arg
NM_001136130.3:c.2030A>G NP_001129602.1:p.His677Arg
NM_001204301.2:c.2144A>G NP_001191230.1:p.His715Arg
NM_001204302.2:c.2087A>G NP_001191231.1:p.His696Arg
NM_001204303.2:c.1919A>G NP_001191232.1:p.His640Arg
NM_201413.3:c.2141A>G NP_958816.1:p.His714Arg
NM_201414.3:c.1973A>G NP_958817.1:p.His658Arg
NM_001136131.3:c.1868A>G NP_001129603.1:p.His623Arg
NM_001385253.1:c.2030A>G NP_001372182.1:p.His677Arg