Canonical Allele Identifier: CA409806460
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897629T>A , CM000683.2:g.25897629T>A GRCh38
NC_000021.8:g.27269941T>A , CM000683.1:g.27269941T>A GRCh37
NC_000021.7:g.26191812T>A NCBI36
NG_007376.1:g.278192A>T
NG_007376.2:g.278500A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1975A>T
ENST00000707133.1:n.405A>T
ENST00000707134.1:n.674A>T
ENST00000346798.8:c.2008A>T MANE Select ENSP00000284981.4:p.Lys670Ter
ENST00000346798.7:c.2008A>T ENSP00000284981.4:p.Lys670Ter
ENST00000348990.9:c.1783A>T ENSP00000345463.5:p.Lys595Ter
ENST00000354192.7:c.1615A>T ENSP00000346129.3:p.Lys539Ter
ENST00000357903.7:c.1951A>T ENSP00000350578.3:p.Lys651Ter
ENST00000358918.7:c.1954A>T ENSP00000351796.3:p.Lys652Ter
ENST00000359726.7:c.1678A>T ENSP00000352760.4:p.Lys560Ter
ENST00000439274.6:c.1840A>T ENSP00000398879.2:p.Lys614Ter
ENST00000440126.7:c.1936A>T ENSP00000387483.2:p.Lys646Ter
ENST00000464867.1:n.355A>T
NM_000484.3:c.2008A>T NP_000475.1:p.Lys670Ter
NM_001136016.3:c.1936A>T NP_001129488.1:p.Lys646Ter
NM_001136129.2:c.1615A>T NP_001129601.1:p.Lys539Ter
NM_001136130.2:c.1840A>T NP_001129602.1:p.Lys614Ter
NM_001136131.2:c.1678A>T NP_001129603.1:p.Lys560Ter
NM_001204301.1:c.1954A>T NP_001191230.1:p.Lys652Ter
NM_001204302.1:c.1897A>T NP_001191231.1:p.Lys633Ter
NM_001204303.1:c.1729A>T NP_001191232.1:p.Lys577Ter
NM_201413.2:c.1951A>T NP_958816.1:p.Lys651Ter
NM_201414.2:c.1783A>T NP_958817.1:p.Lys595Ter
NM_000484.4:c.2008A>T MANE Select NP_000475.1:p.Lys670Ter
NM_001136129.3:c.1615A>T NP_001129601.1:p.Lys539Ter
NM_001136130.3:c.1840A>T NP_001129602.1:p.Lys614Ter
NM_001204301.2:c.1954A>T NP_001191230.1:p.Lys652Ter
NM_001204302.2:c.1897A>T NP_001191231.1:p.Lys633Ter
NM_001204303.2:c.1729A>T NP_001191232.1:p.Lys577Ter
NM_201413.3:c.1951A>T NP_958816.1:p.Lys651Ter
NM_201414.3:c.1783A>T NP_958817.1:p.Lys595Ter
NM_001136131.3:c.1678A>T NP_001129603.1:p.Lys560Ter
NM_001385253.1:c.1840A>T NP_001372182.1:p.Lys614Ter