Canonical Allele Identifier: CA409805580
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891802C>A , CM000683.2:g.25891802C>A GRCh38
NC_000021.8:g.27264114C>A , CM000683.1:g.27264114C>A GRCh37
NC_000021.7:g.26185985C>A NCBI36
NG_007376.1:g.284019G>T
NG_007376.2:g.284327G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2098G>T
ENST00000707133.1:n.528G>T
ENST00000707134.1:n.797G>T
ENST00000346798.8:c.2131G>T MANE Select ENSP00000284981.4:p.Val711Phe
ENST00000346798.7:c.2131G>T ENSP00000284981.4:p.Val711Phe
ENST00000348990.9:c.1906G>T ENSP00000345463.5:p.Val636Phe
ENST00000354192.7:c.1738G>T ENSP00000346129.3:p.Val580Phe
ENST00000357903.7:c.2074G>T ENSP00000350578.3:p.Val692Phe
ENST00000358918.7:c.2077G>T ENSP00000351796.3:p.Val693Phe
ENST00000359726.7:c.1801G>T ENSP00000352760.4:p.Val601Phe
ENST00000439274.6:c.1963G>T ENSP00000398879.2:p.Val655Phe
ENST00000440126.7:c.2059G>T ENSP00000387483.2:p.Val687Phe
ENST00000464867.1:n.478G>T
NM_000484.3:c.2131G>T NP_000475.1:p.Val711Phe
NM_001136016.3:c.2059G>T NP_001129488.1:p.Val687Phe
NM_001136129.2:c.1738G>T NP_001129601.1:p.Val580Phe
NM_001136130.2:c.1963G>T NP_001129602.1:p.Val655Phe
NM_001136131.2:c.1801G>T NP_001129603.1:p.Val601Phe
NM_001204301.1:c.2077G>T NP_001191230.1:p.Val693Phe
NM_001204302.1:c.2020G>T NP_001191231.1:p.Val674Phe
NM_001204303.1:c.1852G>T NP_001191232.1:p.Val618Phe
NM_201413.2:c.2074G>T NP_958816.1:p.Val692Phe
NM_201414.2:c.1906G>T NP_958817.1:p.Val636Phe
NM_000484.4:c.2131G>T MANE Select NP_000475.1:p.Val711Phe
NM_001136129.3:c.1738G>T NP_001129601.1:p.Val580Phe
NM_001136130.3:c.1963G>T NP_001129602.1:p.Val655Phe
NM_001204301.2:c.2077G>T NP_001191230.1:p.Val693Phe
NM_001204302.2:c.2020G>T NP_001191231.1:p.Val674Phe
NM_001204303.2:c.1852G>T NP_001191232.1:p.Val618Phe
NM_201413.3:c.2074G>T NP_958816.1:p.Val692Phe
NM_201414.3:c.1906G>T NP_958817.1:p.Val636Phe
NM_001136131.3:c.1801G>T NP_001129603.1:p.Val601Phe
NM_001385253.1:c.1963G>T NP_001372182.1:p.Val655Phe