Canonical Allele Identifier: CA409805471
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891748T>G , CM000683.2:g.25891748T>G GRCh38
NC_000021.8:g.27264060T>G , CM000683.1:g.27264060T>G GRCh37
NC_000021.7:g.26185931T>G NCBI36
NG_007376.1:g.284073A>C
NG_007376.2:g.284381A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2152A>C
ENST00000707133.1:n.582A>C
ENST00000707134.1:n.851A>C
ENST00000346798.8:c.2185A>C MANE Select ENSP00000284981.4:p.Thr729Pro
ENST00000346798.7:c.2185A>C ENSP00000284981.4:p.Thr729Pro
ENST00000348990.9:c.1960A>C ENSP00000345463.5:p.Thr654Pro
ENST00000354192.7:c.1792A>C ENSP00000346129.3:p.Thr598Pro
ENST00000357903.7:c.2128A>C ENSP00000350578.3:p.Thr710Pro
ENST00000358918.7:c.2131A>C ENSP00000351796.3:p.Thr711Pro
ENST00000359726.7:c.1855A>C ENSP00000352760.4:p.Thr619Pro
ENST00000439274.6:c.2017A>C ENSP00000398879.2:p.Thr673Pro
ENST00000440126.7:c.2113A>C ENSP00000387483.2:p.Thr705Pro
ENST00000464867.1:n.532A>C
NM_000484.3:c.2185A>C NP_000475.1:p.Thr729Pro
NM_001136016.3:c.2113A>C NP_001129488.1:p.Thr705Pro
NM_001136129.2:c.1792A>C NP_001129601.1:p.Thr598Pro
NM_001136130.2:c.2017A>C NP_001129602.1:p.Thr673Pro
NM_001136131.2:c.1855A>C NP_001129603.1:p.Thr619Pro
NM_001204301.1:c.2131A>C NP_001191230.1:p.Thr711Pro
NM_001204302.1:c.2074A>C NP_001191231.1:p.Thr692Pro
NM_001204303.1:c.1906A>C NP_001191232.1:p.Thr636Pro
NM_201413.2:c.2128A>C NP_958816.1:p.Thr710Pro
NM_201414.2:c.1960A>C NP_958817.1:p.Thr654Pro
NM_000484.4:c.2185A>C MANE Select NP_000475.1:p.Thr729Pro
NM_001136129.3:c.1792A>C NP_001129601.1:p.Thr598Pro
NM_001136130.3:c.2017A>C NP_001129602.1:p.Thr673Pro
NM_001204301.2:c.2131A>C NP_001191230.1:p.Thr711Pro
NM_001204302.2:c.2074A>C NP_001191231.1:p.Thr692Pro
NM_001204303.2:c.1906A>C NP_001191232.1:p.Thr636Pro
NM_201413.3:c.2128A>C NP_958816.1:p.Thr710Pro
NM_201414.3:c.1960A>C NP_958817.1:p.Thr654Pro
NM_001136131.3:c.1855A>C NP_001129603.1:p.Thr619Pro
NM_001385253.1:c.2017A>C NP_001372182.1:p.Thr673Pro