Canonical Allele Identifier: CA409806231
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897578T>A , CM000683.2:g.25897578T>A GRCh38
NC_000021.8:g.27269890T>A , CM000683.1:g.27269890T>A GRCh37
NC_000021.7:g.26191761T>A NCBI36
NG_007376.1:g.278243A>T
NG_007376.2:g.278551A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2026A>T
ENST00000707133.1:n.456A>T
ENST00000707134.1:n.725A>T
ENST00000346798.8:c.2059A>T MANE Select ENSP00000284981.4:p.Lys687Ter
ENST00000346798.7:c.2059A>T ENSP00000284981.4:p.Lys687Ter
ENST00000348990.9:c.1834A>T ENSP00000345463.5:p.Lys612Ter
ENST00000354192.7:c.1666A>T ENSP00000346129.3:p.Lys556Ter
ENST00000357903.7:c.2002A>T ENSP00000350578.3:p.Lys668Ter
ENST00000358918.7:c.2005A>T ENSP00000351796.3:p.Lys669Ter
ENST00000359726.7:c.1729A>T ENSP00000352760.4:p.Lys577Ter
ENST00000439274.6:c.1891A>T ENSP00000398879.2:p.Lys631Ter
ENST00000440126.7:c.1987A>T ENSP00000387483.2:p.Lys663Ter
ENST00000464867.1:n.406A>T
NM_000484.3:c.2059A>T NP_000475.1:p.Lys687Ter
NM_001136016.3:c.1987A>T NP_001129488.1:p.Lys663Ter
NM_001136129.2:c.1666A>T NP_001129601.1:p.Lys556Ter
NM_001136130.2:c.1891A>T NP_001129602.1:p.Lys631Ter
NM_001136131.2:c.1729A>T NP_001129603.1:p.Lys577Ter
NM_001204301.1:c.2005A>T NP_001191230.1:p.Lys669Ter
NM_001204302.1:c.1948A>T NP_001191231.1:p.Lys650Ter
NM_001204303.1:c.1780A>T NP_001191232.1:p.Lys594Ter
NM_201413.2:c.2002A>T NP_958816.1:p.Lys668Ter
NM_201414.2:c.1834A>T NP_958817.1:p.Lys612Ter
NM_000484.4:c.2059A>T MANE Select NP_000475.1:p.Lys687Ter
NM_001136129.3:c.1666A>T NP_001129601.1:p.Lys556Ter
NM_001136130.3:c.1891A>T NP_001129602.1:p.Lys631Ter
NM_001204301.2:c.2005A>T NP_001191230.1:p.Lys669Ter
NM_001204302.2:c.1948A>T NP_001191231.1:p.Lys650Ter
NM_001204303.2:c.1780A>T NP_001191232.1:p.Lys594Ter
NM_201413.3:c.2002A>T NP_958816.1:p.Lys668Ter
NM_201414.3:c.1834A>T NP_958817.1:p.Lys612Ter
NM_001136131.3:c.1729A>T NP_001129603.1:p.Lys577Ter
NM_001385253.1:c.1891A>T NP_001372182.1:p.Lys631Ter