Canonical Allele Identifier: CA409805684
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891853C>A , CM000683.2:g.25891853C>A GRCh38
NC_000021.8:g.27264165C>A , CM000683.1:g.27264165C>A GRCh37
NC_000021.7:g.26186036C>A NCBI36
NG_007376.1:g.283968G>T
NG_007376.2:g.284276G>T

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2080G>T NP_000475.1:p.Asp694Tyr
NM_001136016.3:c.2008G>T NP_001129488.1:p.Asp670Tyr
NM_001136129.2:c.1687G>T NP_001129601.1:p.Asp563Tyr
NM_001136130.2:c.1912G>T NP_001129602.1:p.Asp638Tyr
NM_001136131.2:c.1750G>T NP_001129603.1:p.Asp584Tyr
NM_001204301.1:c.2026G>T NP_001191230.1:p.Asp676Tyr
NM_001204302.1:c.1969G>T NP_001191231.1:p.Asp657Tyr
NM_001204303.1:c.1801G>T NP_001191232.1:p.Asp601Tyr
NM_201413.2:c.2023G>T NP_958816.1:p.Asp675Tyr
NM_201414.2:c.1855G>T NP_958817.1:p.Asp619Tyr
NM_000484.4:c.2080G>T MANE Select NP_000475.1:p.Asp694Tyr
NM_001136129.3:c.1687G>T NP_001129601.1:p.Asp563Tyr
NM_001136130.3:c.1912G>T NP_001129602.1:p.Asp638Tyr
NM_001204301.2:c.2026G>T NP_001191230.1:p.Asp676Tyr
NM_001204302.2:c.1969G>T NP_001191231.1:p.Asp657Tyr
NM_001204303.2:c.1801G>T NP_001191232.1:p.Asp601Tyr
NM_201413.3:c.2023G>T NP_958816.1:p.Asp675Tyr
NM_201414.3:c.1855G>T NP_958817.1:p.Asp619Tyr
NM_001136131.3:c.1750G>T NP_001129603.1:p.Asp584Tyr
NM_001385253.1:c.1912G>T NP_001372182.1:p.Asp638Tyr
ENST00000346798.7:c.2080G>T ENSP00000284981.4:p.Asp694Tyr
ENST00000348990.9:c.1855G>T ENSP00000345463.5:p.Asp619Tyr
ENST00000354192.7:c.1687G>T ENSP00000346129.3:p.Asp563Tyr
ENST00000357903.7:c.2023G>T ENSP00000350578.3:p.Asp675Tyr
ENST00000358918.7:c.2026G>T ENSP00000351796.3:p.Asp676Tyr
ENST00000359726.7:c.1750G>T ENSP00000352760.4:p.Asp584Tyr
ENST00000439274.6:c.1912G>T ENSP00000398879.2:p.Asp638Tyr
ENST00000440126.7:c.2008G>T ENSP00000387483.2:p.Asp670Tyr
ENST00000464867.1:n.427G>T