Canonical Allele Identifier: CA2383551547
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891641G= , CM000683.2:g.25891641G= GRCh38
NC_000021.8:g.27263953G= , CM000683.1:g.27263953G= GRCh37
NC_000021.7:g.26185824G= NCBI36
NG_007376.1:g.284180C=
NG_007376.2:g.284488C=

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2211+81C= MANE Select ENSP00000284981.4:n.2211+81C=
ENST00000346798.7:c.2211+81C= ENSP00000284981.4:n.2211+81C=
ENST00000348990.9:c.1986+81C= ENSP00000345463.5:n.1986+81C=
ENST00000354192.7:c.1818+81C= ENSP00000346129.3:n.1818+81C=
ENST00000357903.7:c.2154+81C= ENSP00000350578.3:n.2154+81C=
ENST00000358918.7:c.2157+81C= ENSP00000351796.3:n.2157+81C=
ENST00000359726.7:c.1881+81C= ENSP00000352760.4:n.1881+81C=
ENST00000439274.6:c.2043+81C= ENSP00000398879.2:n.2043+81C=
ENST00000440126.7:c.2139+81C= ENSP00000387483.2:n.2139+81C=
ENST00000464867.1:n.558+81C=
NM_000484.3:c.2211+81C= NP_000475.1:n.2211+81C=
NM_001136016.3:c.2139+81C= NP_001129488.1:n.2139+81C=
NM_001136129.2:c.1818+81C= NP_001129601.1:n.1818+81C=
NM_001136130.2:c.2043+81C= NP_001129602.1:n.2043+81C=
NM_001136131.2:c.1881+81C= NP_001129603.1:n.1881+81C=
NM_001204301.1:c.2157+81C= NP_001191230.1:n.2157+81C=
NM_001204302.1:c.2100+81C= NP_001191231.1:n.2100+81C=
NM_001204303.1:c.1932+81C= NP_001191232.1:n.1932+81C=
NM_201413.2:c.2154+81C= NP_958816.1:n.2154+81C=
NM_201414.2:c.1986+81C= NP_958817.1:n.1986+81C=
NM_000484.4:c.2211+81C= MANE Select NP_000475.1:n.2211+81C=
NM_001136129.3:c.1818+81C= NP_001129601.1:n.1818+81C=
NM_001136130.3:c.2043+81C= NP_001129602.1:n.2043+81C=
NM_001204301.2:c.2157+81C= NP_001191230.1:n.2157+81C=
NM_001204302.2:c.2100+81C= NP_001191231.1:n.2100+81C=
NM_001204303.2:c.1932+81C= NP_001191232.1:n.1932+81C=
NM_201413.3:c.2154+81C= NP_958816.1:n.2154+81C=
NM_201414.3:c.1986+81C= NP_958817.1:n.1986+81C=
NM_001136131.3:c.1881+81C= NP_001129603.1:n.1881+81C=
NM_001385253.1:c.2043+81C= NP_001372182.1:n.2043+81C=