Canonical Allele Identifier: CA2383551930
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25892374G= , CM000683.2:g.25892374G= GRCh38
NC_000021.8:g.27264686G= , CM000683.1:g.27264686G= GRCh37
NC_000021.7:g.26186557G= NCBI36
NG_007376.1:g.283447C=
NG_007376.2:g.283755C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2032-506C=
ENST00000707133.1:n.462-506C=
ENST00000707134.1:n.731-506C=
ENST00000346798.8:c.2065-506C= MANE Select ENSP00000284981.4:n.2065-506C=
ENST00000346798.7:c.2065-506C= ENSP00000284981.4:n.2065-506C=
ENST00000348990.9:c.1840-506C= ENSP00000345463.5:n.1840-506C=
ENST00000354192.7:c.1672-506C= ENSP00000346129.3:n.1672-506C=
ENST00000357903.7:c.2008-506C= ENSP00000350578.3:n.2008-506C=
ENST00000358918.7:c.2011-506C= ENSP00000351796.3:n.2011-506C=
ENST00000359726.7:c.1735-506C= ENSP00000352760.4:n.1735-506C=
ENST00000439274.6:c.1897-506C= ENSP00000398879.2:n.1897-506C=
ENST00000440126.7:c.1993-506C= ENSP00000387483.2:n.1993-506C=
ENST00000464867.1:n.412-506C=
NM_000484.3:c.2065-506C= NP_000475.1:n.2065-506C=
NM_001136016.3:c.1993-506C= NP_001129488.1:n.1993-506C=
NM_001136129.2:c.1672-506C= NP_001129601.1:n.1672-506C=
NM_001136130.2:c.1897-506C= NP_001129602.1:n.1897-506C=
NM_001136131.2:c.1735-506C= NP_001129603.1:n.1735-506C=
NM_001204301.1:c.2011-506C= NP_001191230.1:n.2011-506C=
NM_001204302.1:c.1954-506C= NP_001191231.1:n.1954-506C=
NM_001204303.1:c.1786-506C= NP_001191232.1:n.1786-506C=
NM_201413.2:c.2008-506C= NP_958816.1:n.2008-506C=
NM_201414.2:c.1840-506C= NP_958817.1:n.1840-506C=
NM_000484.4:c.2065-506C= MANE Select NP_000475.1:n.2065-506C=
NM_001136129.3:c.1672-506C= NP_001129601.1:n.1672-506C=
NM_001136130.3:c.1897-506C= NP_001129602.1:n.1897-506C=
NM_001204301.2:c.2011-506C= NP_001191230.1:n.2011-506C=
NM_001204302.2:c.1954-506C= NP_001191231.1:n.1954-506C=
NM_001204303.2:c.1786-506C= NP_001191232.1:n.1786-506C=
NM_201413.3:c.2008-506C= NP_958816.1:n.2008-506C=
NM_201414.3:c.1840-506C= NP_958817.1:n.1840-506C=
NM_001136131.3:c.1735-506C= NP_001129603.1:n.1735-506C=
NM_001385253.1:c.1897-506C= NP_001372182.1:n.1897-506C=