Canonical Allele Identifier: CA409806550
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897652T>A , CM000683.2:g.25897652T>A GRCh38
NC_000021.8:g.27269964T>A , CM000683.1:g.27269964T>A GRCh37
NC_000021.7:g.26191835T>A NCBI36
NG_007376.1:g.278169A>T
NG_007376.2:g.278477A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1952A>T
ENST00000707133.1:n.382A>T
ENST00000707134.1:n.651A>T
ENST00000346798.8:c.1985A>T MANE Select ENSP00000284981.4:p.Lys662Met
ENST00000346798.7:c.1985A>T ENSP00000284981.4:p.Lys662Met
ENST00000348990.9:c.1760A>T ENSP00000345463.5:p.Lys587Met
ENST00000354192.7:c.1592A>T ENSP00000346129.3:p.Lys531Met
ENST00000357903.7:c.1928A>T ENSP00000350578.3:p.Lys643Met
ENST00000358918.7:c.1931A>T ENSP00000351796.3:p.Lys644Met
ENST00000359726.7:c.1655A>T ENSP00000352760.4:p.Lys552Met
ENST00000439274.6:c.1817A>T ENSP00000398879.2:p.Lys606Met
ENST00000440126.7:c.1913A>T ENSP00000387483.2:p.Lys638Met
ENST00000464867.1:n.332A>T
NM_000484.3:c.1985A>T NP_000475.1:p.Lys662Met
NM_001136016.3:c.1913A>T NP_001129488.1:p.Lys638Met
NM_001136129.2:c.1592A>T NP_001129601.1:p.Lys531Met
NM_001136130.2:c.1817A>T NP_001129602.1:p.Lys606Met
NM_001136131.2:c.1655A>T NP_001129603.1:p.Lys552Met
NM_001204301.1:c.1931A>T NP_001191230.1:p.Lys644Met
NM_001204302.1:c.1874A>T NP_001191231.1:p.Lys625Met
NM_001204303.1:c.1706A>T NP_001191232.1:p.Lys569Met
NM_201413.2:c.1928A>T NP_958816.1:p.Lys643Met
NM_201414.2:c.1760A>T NP_958817.1:p.Lys587Met
NM_000484.4:c.1985A>T MANE Select NP_000475.1:p.Lys662Met
NM_001136129.3:c.1592A>T NP_001129601.1:p.Lys531Met
NM_001136130.3:c.1817A>T NP_001129602.1:p.Lys606Met
NM_001204301.2:c.1931A>T NP_001191230.1:p.Lys644Met
NM_001204302.2:c.1874A>T NP_001191231.1:p.Lys625Met
NM_001204303.2:c.1706A>T NP_001191232.1:p.Lys569Met
NM_201413.3:c.1928A>T NP_958816.1:p.Lys643Met
NM_201414.3:c.1760A>T NP_958817.1:p.Lys587Met
NM_001136131.3:c.1655A>T NP_001129603.1:p.Lys552Met
NM_001385253.1:c.1817A>T NP_001372182.1:p.Lys606Met