Canonical Allele Identifier: CA409806535
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897646T>G , CM000683.2:g.25897646T>G GRCh38
NC_000021.8:g.27269958T>G , CM000683.1:g.27269958T>G GRCh37
NC_000021.7:g.26191829T>G NCBI36
NG_007376.1:g.278175A>C
NG_007376.2:g.278483A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1958A>C
ENST00000707133.1:n.388A>C
ENST00000707134.1:n.657A>C
ENST00000346798.8:c.1991A>C MANE Select ENSP00000284981.4:p.Glu664Ala
ENST00000346798.7:c.1991A>C ENSP00000284981.4:p.Glu664Ala
ENST00000348990.9:c.1766A>C ENSP00000345463.5:p.Glu589Ala
ENST00000354192.7:c.1598A>C ENSP00000346129.3:p.Glu533Ala
ENST00000357903.7:c.1934A>C ENSP00000350578.3:p.Glu645Ala
ENST00000358918.7:c.1937A>C ENSP00000351796.3:p.Glu646Ala
ENST00000359726.7:c.1661A>C ENSP00000352760.4:p.Glu554Ala
ENST00000439274.6:c.1823A>C ENSP00000398879.2:p.Glu608Ala
ENST00000440126.7:c.1919A>C ENSP00000387483.2:p.Glu640Ala
ENST00000464867.1:n.338A>C
NM_000484.3:c.1991A>C NP_000475.1:p.Glu664Ala
NM_001136016.3:c.1919A>C NP_001129488.1:p.Glu640Ala
NM_001136129.2:c.1598A>C NP_001129601.1:p.Glu533Ala
NM_001136130.2:c.1823A>C NP_001129602.1:p.Glu608Ala
NM_001136131.2:c.1661A>C NP_001129603.1:p.Glu554Ala
NM_001204301.1:c.1937A>C NP_001191230.1:p.Glu646Ala
NM_001204302.1:c.1880A>C NP_001191231.1:p.Glu627Ala
NM_001204303.1:c.1712A>C NP_001191232.1:p.Glu571Ala
NM_201413.2:c.1934A>C NP_958816.1:p.Glu645Ala
NM_201414.2:c.1766A>C NP_958817.1:p.Glu589Ala
NM_000484.4:c.1991A>C MANE Select NP_000475.1:p.Glu664Ala
NM_001136129.3:c.1598A>C NP_001129601.1:p.Glu533Ala
NM_001136130.3:c.1823A>C NP_001129602.1:p.Glu608Ala
NM_001204301.2:c.1937A>C NP_001191230.1:p.Glu646Ala
NM_001204302.2:c.1880A>C NP_001191231.1:p.Glu627Ala
NM_001204303.2:c.1712A>C NP_001191232.1:p.Glu571Ala
NM_201413.3:c.1934A>C NP_958816.1:p.Glu645Ala
NM_201414.3:c.1766A>C NP_958817.1:p.Glu589Ala
NM_001136131.3:c.1661A>C NP_001129603.1:p.Glu554Ala
NM_001385253.1:c.1823A>C NP_001372182.1:p.Glu608Ala