Canonical Allele Identifier: CA409806317
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2009A>C
ENST00000707133.1:n.439A>C
ENST00000707134.1:n.708A>C
ENST00000346798.8:c.2042A>C MANE Select ENSP00000284981.4:p.Tyr681Ser
ENST00000346798.7:c.2042A>C ENSP00000284981.4:p.Tyr681Ser
ENST00000348990.9:c.1817A>C ENSP00000345463.5:p.Tyr606Ser
ENST00000354192.7:c.1649A>C ENSP00000346129.3:p.Tyr550Ser
ENST00000357903.7:c.1985A>C ENSP00000350578.3:p.Tyr662Ser
ENST00000358918.7:c.1988A>C ENSP00000351796.3:p.Tyr663Ser
ENST00000359726.7:c.1712A>C ENSP00000352760.4:p.Tyr571Ser
ENST00000439274.6:c.1874A>C ENSP00000398879.2:p.Tyr625Ser
ENST00000440126.7:c.1970A>C ENSP00000387483.2:p.Tyr657Ser
ENST00000464867.1:n.389A>C
NM_000484.3:c.2042A>C NP_000475.1:p.Tyr681Ser
NM_001136016.3:c.1970A>C NP_001129488.1:p.Tyr657Ser
NM_001136129.2:c.1649A>C NP_001129601.1:p.Tyr550Ser
NM_001136130.2:c.1874A>C NP_001129602.1:p.Tyr625Ser
NM_001136131.2:c.1712A>C NP_001129603.1:p.Tyr571Ser
NM_001204301.1:c.1988A>C NP_001191230.1:p.Tyr663Ser
NM_001204302.1:c.1931A>C NP_001191231.1:p.Tyr644Ser
NM_001204303.1:c.1763A>C NP_001191232.1:p.Tyr588Ser
NM_201413.2:c.1985A>C NP_958816.1:p.Tyr662Ser
NM_201414.2:c.1817A>C NP_958817.1:p.Tyr606Ser
NM_000484.4:c.2042A>C MANE Select NP_000475.1:p.Tyr681Ser
NM_001136129.3:c.1649A>C NP_001129601.1:p.Tyr550Ser
NM_001136130.3:c.1874A>C NP_001129602.1:p.Tyr625Ser
NM_001204301.2:c.1988A>C NP_001191230.1:p.Tyr663Ser
NM_001204302.2:c.1931A>C NP_001191231.1:p.Tyr644Ser
NM_001204303.2:c.1763A>C NP_001191232.1:p.Tyr588Ser
NM_201413.3:c.1985A>C NP_958816.1:p.Tyr662Ser
NM_201414.3:c.1817A>C NP_958817.1:p.Tyr606Ser
NM_001136131.3:c.1712A>C NP_001129603.1:p.Tyr571Ser
NM_001385253.1:c.1874A>C NP_001372182.1:p.Tyr625Ser