Canonical Allele Identifier: CA409806558
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897655A>T , CM000683.2:g.25897655A>T GRCh38
NC_000021.8:g.27269967A>T , CM000683.1:g.27269967A>T GRCh37
NC_000021.7:g.26191838A>T NCBI36
NG_007376.1:g.278166T>A
NG_007376.2:g.278474T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1949T>A
ENST00000707133.1:n.379T>A
ENST00000707134.1:n.648T>A
ENST00000346798.8:c.1982T>A MANE Select ENSP00000284981.4:p.Ile661Asn
ENST00000346798.7:c.1982T>A ENSP00000284981.4:p.Ile661Asn
ENST00000348990.9:c.1757T>A ENSP00000345463.5:p.Ile586Asn
ENST00000354192.7:c.1589T>A ENSP00000346129.3:p.Ile530Asn
ENST00000357903.7:c.1925T>A ENSP00000350578.3:p.Ile642Asn
ENST00000358918.7:c.1928T>A ENSP00000351796.3:p.Ile643Asn
ENST00000359726.7:c.1652T>A ENSP00000352760.4:p.Ile551Asn
ENST00000439274.6:c.1814T>A ENSP00000398879.2:p.Ile605Asn
ENST00000440126.7:c.1910T>A ENSP00000387483.2:p.Ile637Asn
ENST00000464867.1:n.329T>A
NM_000484.3:c.1982T>A NP_000475.1:p.Ile661Asn
NM_001136016.3:c.1910T>A NP_001129488.1:p.Ile637Asn
NM_001136129.2:c.1589T>A NP_001129601.1:p.Ile530Asn
NM_001136130.2:c.1814T>A NP_001129602.1:p.Ile605Asn
NM_001136131.2:c.1652T>A NP_001129603.1:p.Ile551Asn
NM_001204301.1:c.1928T>A NP_001191230.1:p.Ile643Asn
NM_001204302.1:c.1871T>A NP_001191231.1:p.Ile624Asn
NM_001204303.1:c.1703T>A NP_001191232.1:p.Ile568Asn
NM_201413.2:c.1925T>A NP_958816.1:p.Ile642Asn
NM_201414.2:c.1757T>A NP_958817.1:p.Ile586Asn
NM_000484.4:c.1982T>A MANE Select NP_000475.1:p.Ile661Asn
NM_001136129.3:c.1589T>A NP_001129601.1:p.Ile530Asn
NM_001136130.3:c.1814T>A NP_001129602.1:p.Ile605Asn
NM_001204301.2:c.1928T>A NP_001191230.1:p.Ile643Asn
NM_001204302.2:c.1871T>A NP_001191231.1:p.Ile624Asn
NM_001204303.2:c.1703T>A NP_001191232.1:p.Ile568Asn
NM_201413.3:c.1925T>A NP_958816.1:p.Ile642Asn
NM_201414.3:c.1757T>A NP_958817.1:p.Ile586Asn
NM_001136131.3:c.1652T>A NP_001129603.1:p.Ile551Asn
NM_001385253.1:c.1814T>A NP_001372182.1:p.Ile605Asn