Canonical Allele Identifier: CA2383551602
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891746T= , CM000683.2:g.25891746T= GRCh38
NC_000021.8:g.27264058T= , CM000683.1:g.27264058T= GRCh37
NC_000021.7:g.26185929T= NCBI36
NG_007376.1:g.284075A=
NG_007376.2:g.284383A=

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2187A= MANE Select ENSP00000284981.4:p.Thr729=
ENST00000346798.7:c.2187A= ENSP00000284981.4:p.Thr729=
ENST00000348990.9:c.1962A= ENSP00000345463.5:p.Thr654=
ENST00000354192.7:c.1794A= ENSP00000346129.3:p.Thr598=
ENST00000357903.7:c.2130A= ENSP00000350578.3:p.Thr710=
ENST00000358918.7:c.2133A= ENSP00000351796.3:p.Thr711=
ENST00000359726.7:c.1857A= ENSP00000352760.4:p.Thr619=
ENST00000439274.6:c.2019A= ENSP00000398879.2:p.Thr673=
ENST00000440126.7:c.2115A= ENSP00000387483.2:p.Thr705=
ENST00000464867.1:n.534A=
NM_000484.3:c.2187A= NP_000475.1:p.Thr729=
NM_001136016.3:c.2115A= NP_001129488.1:p.Thr705=
NM_001136129.2:c.1794A= NP_001129601.1:p.Thr598=
NM_001136130.2:c.2019A= NP_001129602.1:p.Thr673=
NM_001136131.2:c.1857A= NP_001129603.1:p.Thr619=
NM_001204301.1:c.2133A= NP_001191230.1:p.Thr711=
NM_001204302.1:c.2076A= NP_001191231.1:p.Thr692=
NM_001204303.1:c.1908A= NP_001191232.1:p.Thr636=
NM_201413.2:c.2130A= NP_958816.1:p.Thr710=
NM_201414.2:c.1962A= NP_958817.1:p.Thr654=
NM_000484.4:c.2187A= MANE Select NP_000475.1:p.Thr729=
NM_001136129.3:c.1794A= NP_001129601.1:p.Thr598=
NM_001136130.3:c.2019A= NP_001129602.1:p.Thr673=
NM_001204301.2:c.2133A= NP_001191230.1:p.Thr711=
NM_001204302.2:c.2076A= NP_001191231.1:p.Thr692=
NM_001204303.2:c.1908A= NP_001191232.1:p.Thr636=
NM_201413.3:c.2130A= NP_958816.1:p.Thr710=
NM_201414.3:c.1962A= NP_958817.1:p.Thr654=
NM_001136131.3:c.1857A= NP_001129603.1:p.Thr619=
NM_001385253.1:c.2019A= NP_001372182.1:p.Thr673=