Canonical Allele Identifier: CA409806566
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 1409975
ClinVar RCV Id: RCV001939973
dbSNP Id: rs770773038

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1945A>T
ENST00000707133.1:n.375A>T
ENST00000707134.1:n.644A>T
ENST00000346798.8:c.1978A>T MANE Select ENSP00000284981.4:p.Asn660Tyr
ENST00000346798.7:c.1978A>T ENSP00000284981.4:p.Asn660Tyr
ENST00000348990.9:c.1753A>T ENSP00000345463.5:p.Asn585Tyr
ENST00000354192.7:c.1585A>T ENSP00000346129.3:p.Asn529Tyr
ENST00000357903.7:c.1921A>T ENSP00000350578.3:p.Asn641Tyr
ENST00000358918.7:c.1924A>T ENSP00000351796.3:p.Asn642Tyr
ENST00000359726.7:c.1648A>T ENSP00000352760.4:p.Asn550Tyr
ENST00000439274.6:c.1810A>T ENSP00000398879.2:p.Asn604Tyr
ENST00000440126.7:c.1906A>T ENSP00000387483.2:p.Asn636Tyr
ENST00000464867.1:n.325A>T
NM_000484.3:c.1978A>T NP_000475.1:p.Asn660Tyr
NM_001136016.3:c.1906A>T NP_001129488.1:p.Asn636Tyr
NM_001136129.2:c.1585A>T NP_001129601.1:p.Asn529Tyr
NM_001136130.2:c.1810A>T NP_001129602.1:p.Asn604Tyr
NM_001136131.2:c.1648A>T NP_001129603.1:p.Asn550Tyr
NM_001204301.1:c.1924A>T NP_001191230.1:p.Asn642Tyr
NM_001204302.1:c.1867A>T NP_001191231.1:p.Asn623Tyr
NM_001204303.1:c.1699A>T NP_001191232.1:p.Asn567Tyr
NM_201413.2:c.1921A>T NP_958816.1:p.Asn641Tyr
NM_201414.2:c.1753A>T NP_958817.1:p.Asn585Tyr
NM_000484.4:c.1978A>T MANE Select NP_000475.1:p.Asn660Tyr
NM_001136129.3:c.1585A>T NP_001129601.1:p.Asn529Tyr
NM_001136130.3:c.1810A>T NP_001129602.1:p.Asn604Tyr
NM_001204301.2:c.1924A>T NP_001191230.1:p.Asn642Tyr
NM_001204302.2:c.1867A>T NP_001191231.1:p.Asn623Tyr
NM_001204303.2:c.1699A>T NP_001191232.1:p.Asn567Tyr
NM_201413.3:c.1921A>T NP_958816.1:p.Asn641Tyr
NM_201414.3:c.1753A>T NP_958817.1:p.Asn585Tyr
NM_001136131.3:c.1648A>T NP_001129603.1:p.Asn550Tyr
NM_001385253.1:c.1810A>T NP_001372182.1:p.Asn604Tyr