Canonical Allele Identifier: CA409805467
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891747G>C , CM000683.2:g.25891747G>C GRCh38
NC_000021.8:g.27264059G>C , CM000683.1:g.27264059G>C GRCh37
NC_000021.7:g.26185930G>C NCBI36
NG_007376.1:g.284074C>G
NG_007376.2:g.284382C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2186C>G MANE Select ENSP00000284981.4:p.Thr729Arg
ENST00000346798.7:c.2186C>G ENSP00000284981.4:p.Thr729Arg
ENST00000348990.9:c.1961C>G ENSP00000345463.5:p.Thr654Arg
ENST00000354192.7:c.1793C>G ENSP00000346129.3:p.Thr598Arg
ENST00000357903.7:c.2129C>G ENSP00000350578.3:p.Thr710Arg
ENST00000358918.7:c.2132C>G ENSP00000351796.3:p.Thr711Arg
ENST00000359726.7:c.1856C>G ENSP00000352760.4:p.Thr619Arg
ENST00000439274.6:c.2018C>G ENSP00000398879.2:p.Thr673Arg
ENST00000440126.7:c.2114C>G ENSP00000387483.2:p.Thr705Arg
ENST00000464867.1:n.533C>G
NM_000484.3:c.2186C>G NP_000475.1:p.Thr729Arg
NM_001136016.3:c.2114C>G NP_001129488.1:p.Thr705Arg
NM_001136129.2:c.1793C>G NP_001129601.1:p.Thr598Arg
NM_001136130.2:c.2018C>G NP_001129602.1:p.Thr673Arg
NM_001136131.2:c.1856C>G NP_001129603.1:p.Thr619Arg
NM_001204301.1:c.2132C>G NP_001191230.1:p.Thr711Arg
NM_001204302.1:c.2075C>G NP_001191231.1:p.Thr692Arg
NM_001204303.1:c.1907C>G NP_001191232.1:p.Thr636Arg
NM_201413.2:c.2129C>G NP_958816.1:p.Thr710Arg
NM_201414.2:c.1961C>G NP_958817.1:p.Thr654Arg
NM_000484.4:c.2186C>G MANE Select NP_000475.1:p.Thr729Arg
NM_001136129.3:c.1793C>G NP_001129601.1:p.Thr598Arg
NM_001136130.3:c.2018C>G NP_001129602.1:p.Thr673Arg
NM_001204301.2:c.2132C>G NP_001191230.1:p.Thr711Arg
NM_001204302.2:c.2075C>G NP_001191231.1:p.Thr692Arg
NM_001204303.2:c.1907C>G NP_001191232.1:p.Thr636Arg
NM_201413.3:c.2129C>G NP_958816.1:p.Thr710Arg
NM_201414.3:c.1961C>G NP_958817.1:p.Thr654Arg
NM_001136131.3:c.1856C>G NP_001129603.1:p.Thr619Arg
NM_001385253.1:c.2018C>G NP_001372182.1:p.Thr673Arg