Canonical Allele Identifier: CA409805484
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891753T>G , CM000683.2:g.25891753T>G GRCh38
NC_000021.8:g.27264065T>G , CM000683.1:g.27264065T>G GRCh37
NC_000021.7:g.26185936T>G NCBI36
NG_007376.1:g.284068A>C
NG_007376.2:g.284376A>C

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2180A>C NP_000475.1:p.Gln727Pro
NM_001136016.3:c.2108A>C NP_001129488.1:p.Gln703Pro
NM_001136129.2:c.1787A>C NP_001129601.1:p.Gln596Pro
NM_001136130.2:c.2012A>C NP_001129602.1:p.Gln671Pro
NM_001136131.2:c.1850A>C NP_001129603.1:p.Gln617Pro
NM_001204301.1:c.2126A>C NP_001191230.1:p.Gln709Pro
NM_001204302.1:c.2069A>C NP_001191231.1:p.Gln690Pro
NM_001204303.1:c.1901A>C NP_001191232.1:p.Gln634Pro
NM_201413.2:c.2123A>C NP_958816.1:p.Gln708Pro
NM_201414.2:c.1955A>C NP_958817.1:p.Gln652Pro
NM_000484.4:c.2180A>C MANE Select NP_000475.1:p.Gln727Pro
NM_001136129.3:c.1787A>C NP_001129601.1:p.Gln596Pro
NM_001136130.3:c.2012A>C NP_001129602.1:p.Gln671Pro
NM_001204301.2:c.2126A>C NP_001191230.1:p.Gln709Pro
NM_001204302.2:c.2069A>C NP_001191231.1:p.Gln690Pro
NM_001204303.2:c.1901A>C NP_001191232.1:p.Gln634Pro
NM_201413.3:c.2123A>C NP_958816.1:p.Gln708Pro
NM_201414.3:c.1955A>C NP_958817.1:p.Gln652Pro
NM_001136131.3:c.1850A>C NP_001129603.1:p.Gln617Pro
NM_001385253.1:c.2012A>C NP_001372182.1:p.Gln671Pro
ENST00000346798.7:c.2180A>C ENSP00000284981.4:p.Gln727Pro
ENST00000348990.9:c.1955A>C ENSP00000345463.5:p.Gln652Pro
ENST00000354192.7:c.1787A>C ENSP00000346129.3:p.Gln596Pro
ENST00000357903.7:c.2123A>C ENSP00000350578.3:p.Gln708Pro
ENST00000358918.7:c.2126A>C ENSP00000351796.3:p.Gln709Pro
ENST00000359726.7:c.1850A>C ENSP00000352760.4:p.Gln617Pro
ENST00000439274.6:c.2012A>C ENSP00000398879.2:p.Gln671Pro
ENST00000440126.7:c.2108A>C ENSP00000387483.2:p.Gln703Pro
ENST00000464867.1:n.527A>C