Canonical Allele Identifier: CA409805485
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891754G>A , CM000683.2:g.25891754G>A GRCh38
NC_000021.8:g.27264066G>A , CM000683.1:g.27264066G>A GRCh37
NC_000021.7:g.26185937G>A NCBI36
NG_007376.1:g.284067C>T
NG_007376.2:g.284375C>T

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2179C>T NP_000475.1:p.Gln727Ter
NM_001136016.3:c.2107C>T NP_001129488.1:p.Gln703Ter
NM_001136129.2:c.1786C>T NP_001129601.1:p.Gln596Ter
NM_001136130.2:c.2011C>T NP_001129602.1:p.Gln671Ter
NM_001136131.2:c.1849C>T NP_001129603.1:p.Gln617Ter
NM_001204301.1:c.2125C>T NP_001191230.1:p.Gln709Ter
NM_001204302.1:c.2068C>T NP_001191231.1:p.Gln690Ter
NM_001204303.1:c.1900C>T NP_001191232.1:p.Gln634Ter
NM_201413.2:c.2122C>T NP_958816.1:p.Gln708Ter
NM_201414.2:c.1954C>T NP_958817.1:p.Gln652Ter
NM_000484.4:c.2179C>T MANE Select NP_000475.1:p.Gln727Ter
NM_001136129.3:c.1786C>T NP_001129601.1:p.Gln596Ter
NM_001136130.3:c.2011C>T NP_001129602.1:p.Gln671Ter
NM_001204301.2:c.2125C>T NP_001191230.1:p.Gln709Ter
NM_001204302.2:c.2068C>T NP_001191231.1:p.Gln690Ter
NM_001204303.2:c.1900C>T NP_001191232.1:p.Gln634Ter
NM_201413.3:c.2122C>T NP_958816.1:p.Gln708Ter
NM_201414.3:c.1954C>T NP_958817.1:p.Gln652Ter
NM_001136131.3:c.1849C>T NP_001129603.1:p.Gln617Ter
NM_001385253.1:c.2011C>T NP_001372182.1:p.Gln671Ter
ENST00000346798.7:c.2179C>T ENSP00000284981.4:p.Gln727Ter
ENST00000348990.9:c.1954C>T ENSP00000345463.5:p.Gln652Ter
ENST00000354192.7:c.1786C>T ENSP00000346129.3:p.Gln596Ter
ENST00000357903.7:c.2122C>T ENSP00000350578.3:p.Gln708Ter
ENST00000358918.7:c.2125C>T ENSP00000351796.3:p.Gln709Ter
ENST00000359726.7:c.1849C>T ENSP00000352760.4:p.Gln617Ter
ENST00000439274.6:c.2011C>T ENSP00000398879.2:p.Gln671Ter
ENST00000440126.7:c.2107C>T ENSP00000387483.2:p.Gln703Ter
ENST00000464867.1:n.526C>T