Canonical Allele Identifier: CA9987058
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs745948082

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891814C>T , CM000683.2:g.25891814C>T GRCh38
NC_000021.8:g.27264126C>T , CM000683.1:g.27264126C>T GRCh37
NC_000021.7:g.26185997C>T NCBI36
NG_007376.1:g.284007G>A
NG_007376.2:g.284315G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2086G>A
ENST00000707133.1:n.516G>A
ENST00000707134.1:n.785G>A
ENST00000346798.8:c.2119G>A MANE Select ENSP00000284981.4:p.Val707Met
ENST00000346798.7:c.2119G>A ENSP00000284981.4:p.Val707Met
ENST00000348990.9:c.1894G>A ENSP00000345463.5:p.Val632Met
ENST00000354192.7:c.1726G>A ENSP00000346129.3:p.Val576Met
ENST00000357903.7:c.2062G>A ENSP00000350578.3:p.Val688Met
ENST00000358918.7:c.2065G>A ENSP00000351796.3:p.Val689Met
ENST00000359726.7:c.1789G>A ENSP00000352760.4:p.Val597Met
ENST00000439274.6:c.1951G>A ENSP00000398879.2:p.Val651Met
ENST00000440126.7:c.2047G>A ENSP00000387483.2:p.Val683Met
ENST00000464867.1:n.466G>A
NM_000484.3:c.2119G>A NP_000475.1:p.Val707Met
NM_001136016.3:c.2047G>A NP_001129488.1:p.Val683Met
NM_001136129.2:c.1726G>A NP_001129601.1:p.Val576Met
NM_001136130.2:c.1951G>A NP_001129602.1:p.Val651Met
NM_001136131.2:c.1789G>A NP_001129603.1:p.Val597Met
NM_001204301.1:c.2065G>A NP_001191230.1:p.Val689Met
NM_001204302.1:c.2008G>A NP_001191231.1:p.Val670Met
NM_001204303.1:c.1840G>A NP_001191232.1:p.Val614Met
NM_201413.2:c.2062G>A NP_958816.1:p.Val688Met
NM_201414.2:c.1894G>A NP_958817.1:p.Val632Met
NM_000484.4:c.2119G>A MANE Select NP_000475.1:p.Val707Met
NM_001136129.3:c.1726G>A NP_001129601.1:p.Val576Met
NM_001136130.3:c.1951G>A NP_001129602.1:p.Val651Met
NM_001204301.2:c.2065G>A NP_001191230.1:p.Val689Met
NM_001204302.2:c.2008G>A NP_001191231.1:p.Val670Met
NM_001204303.2:c.1840G>A NP_001191232.1:p.Val614Met
NM_201413.3:c.2062G>A NP_958816.1:p.Val688Met
NM_201414.3:c.1894G>A NP_958817.1:p.Val632Met
NM_001136131.3:c.1789G>A NP_001129603.1:p.Val597Met
NM_001385253.1:c.1951G>A NP_001372182.1:p.Val651Met