Canonical Allele Identifier: CA409806578
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897664A>T , CM000683.2:g.25897664A>T GRCh38
NC_000021.8:g.27269976A>T , CM000683.1:g.27269976A>T GRCh37
NC_000021.7:g.26191847A>T NCBI36
NG_007376.1:g.278157T>A
NG_007376.2:g.278465T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1940T>A
ENST00000707133.1:n.370T>A
ENST00000707134.1:n.639T>A
ENST00000346798.8:c.1973T>A MANE Select ENSP00000284981.4:p.Leu658Ter
ENST00000346798.7:c.1973T>A ENSP00000284981.4:p.Leu658Ter
ENST00000348990.9:c.1748T>A ENSP00000345463.5:p.Leu583Ter
ENST00000354192.7:c.1580T>A ENSP00000346129.3:p.Leu527Ter
ENST00000357903.7:c.1916T>A ENSP00000350578.3:p.Leu639Ter
ENST00000358918.7:c.1919T>A ENSP00000351796.3:p.Leu640Ter
ENST00000359726.7:c.1643T>A ENSP00000352760.4:p.Leu548Ter
ENST00000439274.6:c.1805T>A ENSP00000398879.2:p.Leu602Ter
ENST00000440126.7:c.1901T>A ENSP00000387483.2:p.Leu634Ter
ENST00000464867.1:n.320T>A
NM_000484.3:c.1973T>A NP_000475.1:p.Leu658Ter
NM_001136016.3:c.1901T>A NP_001129488.1:p.Leu634Ter
NM_001136129.2:c.1580T>A NP_001129601.1:p.Leu527Ter
NM_001136130.2:c.1805T>A NP_001129602.1:p.Leu602Ter
NM_001136131.2:c.1643T>A NP_001129603.1:p.Leu548Ter
NM_001204301.1:c.1919T>A NP_001191230.1:p.Leu640Ter
NM_001204302.1:c.1862T>A NP_001191231.1:p.Leu621Ter
NM_001204303.1:c.1694T>A NP_001191232.1:p.Leu565Ter
NM_201413.2:c.1916T>A NP_958816.1:p.Leu639Ter
NM_201414.2:c.1748T>A NP_958817.1:p.Leu583Ter
NM_000484.4:c.1973T>A MANE Select NP_000475.1:p.Leu658Ter
NM_001136129.3:c.1580T>A NP_001129601.1:p.Leu527Ter
NM_001136130.3:c.1805T>A NP_001129602.1:p.Leu602Ter
NM_001204301.2:c.1919T>A NP_001191230.1:p.Leu640Ter
NM_001204302.2:c.1862T>A NP_001191231.1:p.Leu621Ter
NM_001204303.2:c.1694T>A NP_001191232.1:p.Leu565Ter
NM_201413.3:c.1916T>A NP_958816.1:p.Leu639Ter
NM_201414.3:c.1748T>A NP_958817.1:p.Leu583Ter
NM_001136131.3:c.1643T>A NP_001129603.1:p.Leu548Ter
NM_001385253.1:c.1805T>A NP_001372182.1:p.Leu602Ter