Canonical Allele Identifier: CA409805565
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891795G>C , CM000683.2:g.25891795G>C GRCh38
NC_000021.8:g.27264107G>C , CM000683.1:g.27264107G>C GRCh37
NC_000021.7:g.26185978G>C NCBI36
NG_007376.1:g.284026C>G
NG_007376.2:g.284334C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2105C>G
ENST00000707133.1:n.535C>G
ENST00000707134.1:n.804C>G
ENST00000346798.8:c.2138C>G MANE Select ENSP00000284981.4:p.Ala713Gly
ENST00000346798.7:c.2138C>G ENSP00000284981.4:p.Ala713Gly
ENST00000348990.9:c.1913C>G ENSP00000345463.5:p.Ala638Gly
ENST00000354192.7:c.1745C>G ENSP00000346129.3:p.Ala582Gly
ENST00000357903.7:c.2081C>G ENSP00000350578.3:p.Ala694Gly
ENST00000358918.7:c.2084C>G ENSP00000351796.3:p.Ala695Gly
ENST00000359726.7:c.1808C>G ENSP00000352760.4:p.Ala603Gly
ENST00000439274.6:c.1970C>G ENSP00000398879.2:p.Ala657Gly
ENST00000440126.7:c.2066C>G ENSP00000387483.2:p.Ala689Gly
ENST00000464867.1:n.485C>G
NM_000484.3:c.2138C>G NP_000475.1:p.Ala713Gly
NM_001136016.3:c.2066C>G NP_001129488.1:p.Ala689Gly
NM_001136129.2:c.1745C>G NP_001129601.1:p.Ala582Gly
NM_001136130.2:c.1970C>G NP_001129602.1:p.Ala657Gly
NM_001136131.2:c.1808C>G NP_001129603.1:p.Ala603Gly
NM_001204301.1:c.2084C>G NP_001191230.1:p.Ala695Gly
NM_001204302.1:c.2027C>G NP_001191231.1:p.Ala676Gly
NM_001204303.1:c.1859C>G NP_001191232.1:p.Ala620Gly
NM_201413.2:c.2081C>G NP_958816.1:p.Ala694Gly
NM_201414.2:c.1913C>G NP_958817.1:p.Ala638Gly
NM_000484.4:c.2138C>G MANE Select NP_000475.1:p.Ala713Gly
NM_001136129.3:c.1745C>G NP_001129601.1:p.Ala582Gly
NM_001136130.3:c.1970C>G NP_001129602.1:p.Ala657Gly
NM_001204301.2:c.2084C>G NP_001191230.1:p.Ala695Gly
NM_001204302.2:c.2027C>G NP_001191231.1:p.Ala676Gly
NM_001204303.2:c.1859C>G NP_001191232.1:p.Ala620Gly
NM_201413.3:c.2081C>G NP_958816.1:p.Ala694Gly
NM_201414.3:c.1913C>G NP_958817.1:p.Ala638Gly
NM_001136131.3:c.1808C>G NP_001129603.1:p.Ala603Gly
NM_001385253.1:c.1970C>G NP_001372182.1:p.Ala657Gly