Canonical Allele Identifier: CA409806565
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs1439246491

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897658T>G , CM000683.2:g.25897658T>G GRCh38
NC_000021.8:g.27269970T>G , CM000683.1:g.27269970T>G GRCh37
NC_000021.7:g.26191841T>G NCBI36
NG_007376.1:g.278163A>C
NG_007376.2:g.278471A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1946A>C
ENST00000707133.1:n.376A>C
ENST00000707134.1:n.645A>C
ENST00000346798.8:c.1979A>C MANE Select ENSP00000284981.4:p.Asn660Thr
ENST00000346798.7:c.1979A>C ENSP00000284981.4:p.Asn660Thr
ENST00000348990.9:c.1754A>C ENSP00000345463.5:p.Asn585Thr
ENST00000354192.7:c.1586A>C ENSP00000346129.3:p.Asn529Thr
ENST00000357903.7:c.1922A>C ENSP00000350578.3:p.Asn641Thr
ENST00000358918.7:c.1925A>C ENSP00000351796.3:p.Asn642Thr
ENST00000359726.7:c.1649A>C ENSP00000352760.4:p.Asn550Thr
ENST00000439274.6:c.1811A>C ENSP00000398879.2:p.Asn604Thr
ENST00000440126.7:c.1907A>C ENSP00000387483.2:p.Asn636Thr
ENST00000464867.1:n.326A>C
NM_000484.3:c.1979A>C NP_000475.1:p.Asn660Thr
NM_001136016.3:c.1907A>C NP_001129488.1:p.Asn636Thr
NM_001136129.2:c.1586A>C NP_001129601.1:p.Asn529Thr
NM_001136130.2:c.1811A>C NP_001129602.1:p.Asn604Thr
NM_001136131.2:c.1649A>C NP_001129603.1:p.Asn550Thr
NM_001204301.1:c.1925A>C NP_001191230.1:p.Asn642Thr
NM_001204302.1:c.1868A>C NP_001191231.1:p.Asn623Thr
NM_001204303.1:c.1700A>C NP_001191232.1:p.Asn567Thr
NM_201413.2:c.1922A>C NP_958816.1:p.Asn641Thr
NM_201414.2:c.1754A>C NP_958817.1:p.Asn585Thr
NM_000484.4:c.1979A>C MANE Select NP_000475.1:p.Asn660Thr
NM_001136129.3:c.1586A>C NP_001129601.1:p.Asn529Thr
NM_001136130.3:c.1811A>C NP_001129602.1:p.Asn604Thr
NM_001204301.2:c.1925A>C NP_001191230.1:p.Asn642Thr
NM_001204302.2:c.1868A>C NP_001191231.1:p.Asn623Thr
NM_001204303.2:c.1700A>C NP_001191232.1:p.Asn567Thr
NM_201413.3:c.1922A>C NP_958816.1:p.Asn641Thr
NM_201414.3:c.1754A>C NP_958817.1:p.Asn585Thr
NM_001136131.3:c.1649A>C NP_001129603.1:p.Asn550Thr
NM_001385253.1:c.1811A>C NP_001372182.1:p.Asn604Thr