Canonical Allele Identifier: CA409805654
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891839G>T , CM000683.2:g.25891839G>T GRCh38
NC_000021.8:g.27264151G>T , CM000683.1:g.27264151G>T GRCh37
NC_000021.7:g.26186022G>T NCBI36
NG_007376.1:g.283982C>A
NG_007376.2:g.284290C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2061C>A
ENST00000707133.1:n.491C>A
ENST00000707134.1:n.760C>A
ENST00000346798.8:c.2094C>A MANE Select ENSP00000284981.4:p.Asn698Lys
ENST00000346798.7:c.2094C>A ENSP00000284981.4:p.Asn698Lys
ENST00000348990.9:c.1869C>A ENSP00000345463.5:p.Asn623Lys
ENST00000354192.7:c.1701C>A ENSP00000346129.3:p.Asn567Lys
ENST00000357903.7:c.2037C>A ENSP00000350578.3:p.Asn679Lys
ENST00000358918.7:c.2040C>A ENSP00000351796.3:p.Asn680Lys
ENST00000359726.7:c.1764C>A ENSP00000352760.4:p.Asn588Lys
ENST00000439274.6:c.1926C>A ENSP00000398879.2:p.Asn642Lys
ENST00000440126.7:c.2022C>A ENSP00000387483.2:p.Asn674Lys
ENST00000464867.1:n.441C>A
NM_000484.3:c.2094C>A NP_000475.1:p.Asn698Lys
NM_001136016.3:c.2022C>A NP_001129488.1:p.Asn674Lys
NM_001136129.2:c.1701C>A NP_001129601.1:p.Asn567Lys
NM_001136130.2:c.1926C>A NP_001129602.1:p.Asn642Lys
NM_001136131.2:c.1764C>A NP_001129603.1:p.Asn588Lys
NM_001204301.1:c.2040C>A NP_001191230.1:p.Asn680Lys
NM_001204302.1:c.1983C>A NP_001191231.1:p.Asn661Lys
NM_001204303.1:c.1815C>A NP_001191232.1:p.Asn605Lys
NM_201413.2:c.2037C>A NP_958816.1:p.Asn679Lys
NM_201414.2:c.1869C>A NP_958817.1:p.Asn623Lys
NM_000484.4:c.2094C>A MANE Select NP_000475.1:p.Asn698Lys
NM_001136129.3:c.1701C>A NP_001129601.1:p.Asn567Lys
NM_001136130.3:c.1926C>A NP_001129602.1:p.Asn642Lys
NM_001204301.2:c.2040C>A NP_001191230.1:p.Asn680Lys
NM_001204302.2:c.1983C>A NP_001191231.1:p.Asn661Lys
NM_001204303.2:c.1815C>A NP_001191232.1:p.Asn605Lys
NM_201413.3:c.2037C>A NP_958816.1:p.Asn679Lys
NM_201414.3:c.1869C>A NP_958817.1:p.Asn623Lys
NM_001136131.3:c.1764C>A NP_001129603.1:p.Asn588Lys
NM_001385253.1:c.1926C>A NP_001372182.1:p.Asn642Lys