Canonical Allele Identifier: CA409806555
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897653T>C , CM000683.2:g.25897653T>C GRCh38
NC_000021.8:g.27269965T>C , CM000683.1:g.27269965T>C GRCh37
NC_000021.7:g.26191836T>C NCBI36
NG_007376.1:g.278168A>G
NG_007376.2:g.278476A>G

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.1984A>G NP_000475.1:p.Lys662Glu
NM_001136016.3:c.1912A>G NP_001129488.1:p.Lys638Glu
NM_001136129.2:c.1591A>G NP_001129601.1:p.Lys531Glu
NM_001136130.2:c.1816A>G NP_001129602.1:p.Lys606Glu
NM_001136131.2:c.1654A>G NP_001129603.1:p.Lys552Glu
NM_001204301.1:c.1930A>G NP_001191230.1:p.Lys644Glu
NM_001204302.1:c.1873A>G NP_001191231.1:p.Lys625Glu
NM_001204303.1:c.1705A>G NP_001191232.1:p.Lys569Glu
NM_201413.2:c.1927A>G NP_958816.1:p.Lys643Glu
NM_201414.2:c.1759A>G NP_958817.1:p.Lys587Glu
NM_000484.4:c.1984A>G MANE Select NP_000475.1:p.Lys662Glu
NM_001136129.3:c.1591A>G NP_001129601.1:p.Lys531Glu
NM_001136130.3:c.1816A>G NP_001129602.1:p.Lys606Glu
NM_001204301.2:c.1930A>G NP_001191230.1:p.Lys644Glu
NM_001204302.2:c.1873A>G NP_001191231.1:p.Lys625Glu
NM_001204303.2:c.1705A>G NP_001191232.1:p.Lys569Glu
NM_201413.3:c.1927A>G NP_958816.1:p.Lys643Glu
NM_201414.3:c.1759A>G NP_958817.1:p.Lys587Glu
NM_001136131.3:c.1654A>G NP_001129603.1:p.Lys552Glu
NM_001385253.1:c.1816A>G NP_001372182.1:p.Lys606Glu
ENST00000346798.7:c.1984A>G ENSP00000284981.4:p.Lys662Glu
ENST00000348990.9:c.1759A>G ENSP00000345463.5:p.Lys587Glu
ENST00000354192.7:c.1591A>G ENSP00000346129.3:p.Lys531Glu
ENST00000357903.7:c.1927A>G ENSP00000350578.3:p.Lys643Glu
ENST00000358918.7:c.1930A>G ENSP00000351796.3:p.Lys644Glu
ENST00000359726.7:c.1654A>G ENSP00000352760.4:p.Lys552Glu
ENST00000439274.6:c.1816A>G ENSP00000398879.2:p.Lys606Glu
ENST00000440126.7:c.1912A>G ENSP00000387483.2:p.Lys638Glu
ENST00000464867.1:n.331A>G