Canonical Allele Identifier: CA409805532
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891774A>T , CM000683.2:g.25891774A>T GRCh38
NC_000021.8:g.27264086A>T , CM000683.1:g.27264086A>T GRCh37
NC_000021.7:g.26185957A>T NCBI36
NG_007376.1:g.284047T>A
NG_007376.2:g.284355T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2126T>A
ENST00000707133.1:n.556T>A
ENST00000707134.1:n.825T>A
ENST00000346798.8:c.2159T>A MANE Select ENSP00000284981.4:p.Leu720Ter
ENST00000346798.7:c.2159T>A ENSP00000284981.4:p.Leu720Ter
ENST00000348990.9:c.1934T>A ENSP00000345463.5:p.Leu645Ter
ENST00000354192.7:c.1766T>A ENSP00000346129.3:p.Leu589Ter
ENST00000357903.7:c.2102T>A ENSP00000350578.3:p.Leu701Ter
ENST00000358918.7:c.2105T>A ENSP00000351796.3:p.Leu702Ter
ENST00000359726.7:c.1829T>A ENSP00000352760.4:p.Leu610Ter
ENST00000439274.6:c.1991T>A ENSP00000398879.2:p.Leu664Ter
ENST00000440126.7:c.2087T>A ENSP00000387483.2:p.Leu696Ter
ENST00000464867.1:n.506T>A
NM_000484.3:c.2159T>A NP_000475.1:p.Leu720Ter
NM_001136016.3:c.2087T>A NP_001129488.1:p.Leu696Ter
NM_001136129.2:c.1766T>A NP_001129601.1:p.Leu589Ter
NM_001136130.2:c.1991T>A NP_001129602.1:p.Leu664Ter
NM_001136131.2:c.1829T>A NP_001129603.1:p.Leu610Ter
NM_001204301.1:c.2105T>A NP_001191230.1:p.Leu702Ter
NM_001204302.1:c.2048T>A NP_001191231.1:p.Leu683Ter
NM_001204303.1:c.1880T>A NP_001191232.1:p.Leu627Ter
NM_201413.2:c.2102T>A NP_958816.1:p.Leu701Ter
NM_201414.2:c.1934T>A NP_958817.1:p.Leu645Ter
NM_000484.4:c.2159T>A MANE Select NP_000475.1:p.Leu720Ter
NM_001136129.3:c.1766T>A NP_001129601.1:p.Leu589Ter
NM_001136130.3:c.1991T>A NP_001129602.1:p.Leu664Ter
NM_001204301.2:c.2105T>A NP_001191230.1:p.Leu702Ter
NM_001204302.2:c.2048T>A NP_001191231.1:p.Leu683Ter
NM_001204303.2:c.1880T>A NP_001191232.1:p.Leu627Ter
NM_201413.3:c.2102T>A NP_958816.1:p.Leu701Ter
NM_201414.3:c.1934T>A NP_958817.1:p.Leu645Ter
NM_001136131.3:c.1829T>A NP_001129603.1:p.Leu610Ter
NM_001385253.1:c.1991T>A NP_001372182.1:p.Leu664Ter