Canonical Allele Identifier: CA2383551618
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891792G= , CM000683.2:g.25891792G= GRCh38
NC_000021.8:g.27264104G= , CM000683.1:g.27264104G= GRCh37
NC_000021.7:g.26185975G= NCBI36
NG_007376.1:g.284029C=
NG_007376.2:g.284337C=

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2108C=
ENST00000707133.1:n.538C=
ENST00000707134.1:n.807C=
ENST00000346798.8:c.2141C= MANE Select ENSP00000284981.4:p.Thr714=
ENST00000346798.7:c.2141C= ENSP00000284981.4:p.Thr714=
ENST00000348990.9:c.1916C= ENSP00000345463.5:p.Thr639=
ENST00000354192.7:c.1748C= ENSP00000346129.3:p.Thr583=
ENST00000357903.7:c.2084C= ENSP00000350578.3:p.Thr695=
ENST00000358918.7:c.2087C= ENSP00000351796.3:p.Thr696=
ENST00000359726.7:c.1811C= ENSP00000352760.4:p.Thr604=
ENST00000439274.6:c.1973C= ENSP00000398879.2:p.Thr658=
ENST00000440126.7:c.2069C= ENSP00000387483.2:p.Thr690=
ENST00000464867.1:n.488C=
NM_000484.3:c.2141C= NP_000475.1:p.Thr714=
NM_001136016.3:c.2069C= NP_001129488.1:p.Thr690=
NM_001136129.2:c.1748C= NP_001129601.1:p.Thr583=
NM_001136130.2:c.1973C= NP_001129602.1:p.Thr658=
NM_001136131.2:c.1811C= NP_001129603.1:p.Thr604=
NM_001204301.1:c.2087C= NP_001191230.1:p.Thr696=
NM_001204302.1:c.2030C= NP_001191231.1:p.Thr677=
NM_001204303.1:c.1862C= NP_001191232.1:p.Thr621=
NM_201413.2:c.2084C= NP_958816.1:p.Thr695=
NM_201414.2:c.1916C= NP_958817.1:p.Thr639=
NM_000484.4:c.2141C= MANE Select NP_000475.1:p.Thr714=
NM_001136129.3:c.1748C= NP_001129601.1:p.Thr583=
NM_001136130.3:c.1973C= NP_001129602.1:p.Thr658=
NM_001204301.2:c.2087C= NP_001191230.1:p.Thr696=
NM_001204302.2:c.2030C= NP_001191231.1:p.Thr677=
NM_001204303.2:c.1862C= NP_001191232.1:p.Thr621=
NM_201413.3:c.2084C= NP_958816.1:p.Thr695=
NM_201414.3:c.1916C= NP_958817.1:p.Thr639=
NM_001136131.3:c.1811C= NP_001129603.1:p.Thr604=
NM_001385253.1:c.1973C= NP_001372182.1:p.Thr658=