Canonical Allele Identifier: CA090906
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18094
dbSNP Id: rs63750066

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891796C>T , CM000683.2:g.25891796C>T GRCh38
NC_000021.8:g.27264108C>T , CM000683.1:g.27264108C>T GRCh37
NC_000021.7:g.26185979C>T NCBI36
NG_007376.1:g.284025G>A
NG_007376.2:g.284333G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2104G>A
ENST00000707133.1:n.534G>A
ENST00000707134.1:n.803G>A
ENST00000346798.8:c.2137G>A MANE Select ENSP00000284981.4:p.Ala713Thr
ENST00000346798.7:c.2137G>A ENSP00000284981.4:p.Ala713Thr
ENST00000348990.9:c.1912G>A ENSP00000345463.5:p.Ala638Thr
ENST00000354192.7:c.1744G>A ENSP00000346129.3:p.Ala582Thr
ENST00000357903.7:c.2080G>A ENSP00000350578.3:p.Ala694Thr
ENST00000358918.7:c.2083G>A ENSP00000351796.3:p.Ala695Thr
ENST00000359726.7:c.1807G>A ENSP00000352760.4:p.Ala603Thr
ENST00000439274.6:c.1969G>A ENSP00000398879.2:p.Ala657Thr
ENST00000440126.7:c.2065G>A ENSP00000387483.2:p.Ala689Thr
ENST00000464867.1:n.484G>A
NM_000484.3:c.2137G>A NP_000475.1:p.Ala713Thr
NM_001136016.3:c.2065G>A NP_001129488.1:p.Ala689Thr
NM_001136129.2:c.1744G>A NP_001129601.1:p.Ala582Thr
NM_001136130.2:c.1969G>A NP_001129602.1:p.Ala657Thr
NM_001136131.2:c.1807G>A NP_001129603.1:p.Ala603Thr
NM_001204301.1:c.2083G>A NP_001191230.1:p.Ala695Thr
NM_001204302.1:c.2026G>A NP_001191231.1:p.Ala676Thr
NM_001204303.1:c.1858G>A NP_001191232.1:p.Ala620Thr
NM_201413.2:c.2080G>A NP_958816.1:p.Ala694Thr
NM_201414.2:c.1912G>A NP_958817.1:p.Ala638Thr
NM_000484.4:c.2137G>A MANE Select NP_000475.1:p.Ala713Thr
NM_001136129.3:c.1744G>A NP_001129601.1:p.Ala582Thr
NM_001136130.3:c.1969G>A NP_001129602.1:p.Ala657Thr
NM_001204301.2:c.2083G>A NP_001191230.1:p.Ala695Thr
NM_001204302.2:c.2026G>A NP_001191231.1:p.Ala676Thr
NM_001204303.2:c.1858G>A NP_001191232.1:p.Ala620Thr
NM_201413.3:c.2080G>A NP_958816.1:p.Ala694Thr
NM_201414.3:c.1912G>A NP_958817.1:p.Ala638Thr
NM_001136131.3:c.1807G>A NP_001129603.1:p.Ala603Thr
NM_001385253.1:c.1969G>A NP_001372182.1:p.Ala657Thr