Canonical Allele Identifier: CA409806567
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs770773038

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897659T>C , CM000683.2:g.25897659T>C GRCh38
NC_000021.8:g.27269971T>C , CM000683.1:g.27269971T>C GRCh37
NC_000021.7:g.26191842T>C NCBI36
NG_007376.1:g.278162A>G
NG_007376.2:g.278470A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1945A>G
ENST00000707133.1:n.375A>G
ENST00000707134.1:n.644A>G
ENST00000346798.8:c.1978A>G MANE Select ENSP00000284981.4:p.Asn660Asp
ENST00000346798.7:c.1978A>G ENSP00000284981.4:p.Asn660Asp
ENST00000348990.9:c.1753A>G ENSP00000345463.5:p.Asn585Asp
ENST00000354192.7:c.1585A>G ENSP00000346129.3:p.Asn529Asp
ENST00000357903.7:c.1921A>G ENSP00000350578.3:p.Asn641Asp
ENST00000358918.7:c.1924A>G ENSP00000351796.3:p.Asn642Asp
ENST00000359726.7:c.1648A>G ENSP00000352760.4:p.Asn550Asp
ENST00000439274.6:c.1810A>G ENSP00000398879.2:p.Asn604Asp
ENST00000440126.7:c.1906A>G ENSP00000387483.2:p.Asn636Asp
ENST00000464867.1:n.325A>G
NM_000484.3:c.1978A>G NP_000475.1:p.Asn660Asp
NM_001136016.3:c.1906A>G NP_001129488.1:p.Asn636Asp
NM_001136129.2:c.1585A>G NP_001129601.1:p.Asn529Asp
NM_001136130.2:c.1810A>G NP_001129602.1:p.Asn604Asp
NM_001136131.2:c.1648A>G NP_001129603.1:p.Asn550Asp
NM_001204301.1:c.1924A>G NP_001191230.1:p.Asn642Asp
NM_001204302.1:c.1867A>G NP_001191231.1:p.Asn623Asp
NM_001204303.1:c.1699A>G NP_001191232.1:p.Asn567Asp
NM_201413.2:c.1921A>G NP_958816.1:p.Asn641Asp
NM_201414.2:c.1753A>G NP_958817.1:p.Asn585Asp
NM_000484.4:c.1978A>G MANE Select NP_000475.1:p.Asn660Asp
NM_001136129.3:c.1585A>G NP_001129601.1:p.Asn529Asp
NM_001136130.3:c.1810A>G NP_001129602.1:p.Asn604Asp
NM_001204301.2:c.1924A>G NP_001191230.1:p.Asn642Asp
NM_001204302.2:c.1867A>G NP_001191231.1:p.Asn623Asp
NM_001204303.2:c.1699A>G NP_001191232.1:p.Asn567Asp
NM_201413.3:c.1921A>G NP_958816.1:p.Asn641Asp
NM_201414.3:c.1753A>G NP_958817.1:p.Asn585Asp
NM_001136131.3:c.1648A>G NP_001129603.1:p.Asn550Asp
NM_001385253.1:c.1810A>G NP_001372182.1:p.Asn604Asp