Canonical Allele Identifier: CA130092
Gene: APP HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 37145
dbSNP Id: rs63750847

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897620C>T , CM000683.2:g.25897620C>T GRCh38
NC_000021.8:g.27269932C>T , CM000683.1:g.27269932C>T GRCh37
NC_000021.7:g.26191803C>T NCBI36
NG_007376.1:g.278201G>A
NG_007376.2:g.278509G>A

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2017G>A VV NP_000475.1:p.Ala673Thr
NM_001136016.3:c.1945G>A VV NP_001129488.1:p.Ala649Thr
NM_001136129.2:c.1624G>A VV NP_001129601.1:p.Ala542Thr
NM_001136130.2:c.1849G>A VV NP_001129602.1:p.Ala617Thr
NM_001136131.2:c.1687G>A VV NP_001129603.1:p.Ala563Thr
NM_001204301.1:c.1963G>A VV NP_001191230.1:p.Ala655Thr
NM_001204302.1:c.1906G>A VV NP_001191231.1:p.Ala636Thr
NM_001204303.1:c.1738G>A VV NP_001191232.1:p.Ala580Thr
NM_201413.2:c.1960G>A VV NP_958816.1:p.Ala654Thr
NM_201414.2:c.1792G>A VV NP_958817.1:p.Ala598Thr
NM_000484.4:c.2017G>A VV MANE Preferred
ENST00000346798.7:c.2017G>A ENSP00000284981.4:p.Ala673Thr
ENST00000348990.9:c.1792G>A ENSP00000345463.5:p.Ala598Thr
ENST00000354192.7:c.1624G>A ENSP00000346129.3:p.Ala542Thr
ENST00000357903.7:c.1960G>A ENSP00000350578.3:p.Ala654Thr
ENST00000358918.7:c.1963G>A ENSP00000351796.3:p.Ala655Thr
ENST00000359726.7:c.1687G>A ENSP00000352760.4:p.Ala563Thr
ENST00000439274.6:c.1849G>A ENSP00000398879.2:p.Ala617Thr
ENST00000440126.7:c.1945G>A ENSP00000387483.2:p.Ala649Thr
ENST00000464867.1:n.364G>A