Canonical Allele Identifier: CA409806315
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2009A>G
ENST00000707133.1:n.439A>G
ENST00000707134.1:n.708A>G
ENST00000346798.8:c.2042A>G MANE Select ENSP00000284981.4:p.Tyr681Cys
ENST00000346798.7:c.2042A>G ENSP00000284981.4:p.Tyr681Cys
ENST00000348990.9:c.1817A>G ENSP00000345463.5:p.Tyr606Cys
ENST00000354192.7:c.1649A>G ENSP00000346129.3:p.Tyr550Cys
ENST00000357903.7:c.1985A>G ENSP00000350578.3:p.Tyr662Cys
ENST00000358918.7:c.1988A>G ENSP00000351796.3:p.Tyr663Cys
ENST00000359726.7:c.1712A>G ENSP00000352760.4:p.Tyr571Cys
ENST00000439274.6:c.1874A>G ENSP00000398879.2:p.Tyr625Cys
ENST00000440126.7:c.1970A>G ENSP00000387483.2:p.Tyr657Cys
ENST00000464867.1:n.389A>G
NM_000484.3:c.2042A>G NP_000475.1:p.Tyr681Cys
NM_001136016.3:c.1970A>G NP_001129488.1:p.Tyr657Cys
NM_001136129.2:c.1649A>G NP_001129601.1:p.Tyr550Cys
NM_001136130.2:c.1874A>G NP_001129602.1:p.Tyr625Cys
NM_001136131.2:c.1712A>G NP_001129603.1:p.Tyr571Cys
NM_001204301.1:c.1988A>G NP_001191230.1:p.Tyr663Cys
NM_001204302.1:c.1931A>G NP_001191231.1:p.Tyr644Cys
NM_001204303.1:c.1763A>G NP_001191232.1:p.Tyr588Cys
NM_201413.2:c.1985A>G NP_958816.1:p.Tyr662Cys
NM_201414.2:c.1817A>G NP_958817.1:p.Tyr606Cys
NM_000484.4:c.2042A>G MANE Select NP_000475.1:p.Tyr681Cys
NM_001136129.3:c.1649A>G NP_001129601.1:p.Tyr550Cys
NM_001136130.3:c.1874A>G NP_001129602.1:p.Tyr625Cys
NM_001204301.2:c.1988A>G NP_001191230.1:p.Tyr663Cys
NM_001204302.2:c.1931A>G NP_001191231.1:p.Tyr644Cys
NM_001204303.2:c.1763A>G NP_001191232.1:p.Tyr588Cys
NM_201413.3:c.1985A>G NP_958816.1:p.Tyr662Cys
NM_201414.3:c.1817A>G NP_958817.1:p.Tyr606Cys
NM_001136131.3:c.1712A>G NP_001129603.1:p.Tyr571Cys
NM_001385253.1:c.1874A>G NP_001372182.1:p.Tyr625Cys