Canonical Allele Identifier: CA409806314
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897595T>A , CM000683.2:g.25897595T>A GRCh38
NC_000021.8:g.27269907T>A , CM000683.1:g.27269907T>A GRCh37
NC_000021.7:g.26191778T>A NCBI36
NG_007376.1:g.278226A>T
NG_007376.2:g.278534A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2009A>T
ENST00000707133.1:n.439A>T
ENST00000707134.1:n.708A>T
ENST00000346798.8:c.2042A>T MANE Select ENSP00000284981.4:p.Tyr681Phe
ENST00000346798.7:c.2042A>T ENSP00000284981.4:p.Tyr681Phe
ENST00000348990.9:c.1817A>T ENSP00000345463.5:p.Tyr606Phe
ENST00000354192.7:c.1649A>T ENSP00000346129.3:p.Tyr550Phe
ENST00000357903.7:c.1985A>T ENSP00000350578.3:p.Tyr662Phe
ENST00000358918.7:c.1988A>T ENSP00000351796.3:p.Tyr663Phe
ENST00000359726.7:c.1712A>T ENSP00000352760.4:p.Tyr571Phe
ENST00000439274.6:c.1874A>T ENSP00000398879.2:p.Tyr625Phe
ENST00000440126.7:c.1970A>T ENSP00000387483.2:p.Tyr657Phe
ENST00000464867.1:n.389A>T
NM_000484.3:c.2042A>T NP_000475.1:p.Tyr681Phe
NM_001136016.3:c.1970A>T NP_001129488.1:p.Tyr657Phe
NM_001136129.2:c.1649A>T NP_001129601.1:p.Tyr550Phe
NM_001136130.2:c.1874A>T NP_001129602.1:p.Tyr625Phe
NM_001136131.2:c.1712A>T NP_001129603.1:p.Tyr571Phe
NM_001204301.1:c.1988A>T NP_001191230.1:p.Tyr663Phe
NM_001204302.1:c.1931A>T NP_001191231.1:p.Tyr644Phe
NM_001204303.1:c.1763A>T NP_001191232.1:p.Tyr588Phe
NM_201413.2:c.1985A>T NP_958816.1:p.Tyr662Phe
NM_201414.2:c.1817A>T NP_958817.1:p.Tyr606Phe
NM_000484.4:c.2042A>T MANE Select NP_000475.1:p.Tyr681Phe
NM_001136129.3:c.1649A>T NP_001129601.1:p.Tyr550Phe
NM_001136130.3:c.1874A>T NP_001129602.1:p.Tyr625Phe
NM_001204301.2:c.1988A>T NP_001191230.1:p.Tyr663Phe
NM_001204302.2:c.1931A>T NP_001191231.1:p.Tyr644Phe
NM_001204303.2:c.1763A>T NP_001191232.1:p.Tyr588Phe
NM_201413.3:c.1985A>T NP_958816.1:p.Tyr662Phe
NM_201414.3:c.1817A>T NP_958817.1:p.Tyr606Phe
NM_001136131.3:c.1712A>T NP_001129603.1:p.Tyr571Phe
NM_001385253.1:c.1874A>T NP_001372182.1:p.Tyr625Phe