Canonical Allele Identifier: CA409806336
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897601G>C , CM000683.2:g.25897601G>C GRCh38
NC_000021.8:g.27269913G>C , CM000683.1:g.27269913G>C GRCh37
NC_000021.7:g.26191784G>C NCBI36
NG_007376.1:g.278220C>G
NG_007376.2:g.278528C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2003C>G
ENST00000707133.1:n.433C>G
ENST00000707134.1:n.702C>G
ENST00000346798.8:c.2036C>G MANE Select ENSP00000284981.4:p.Ser679Ter
ENST00000346798.7:c.2036C>G ENSP00000284981.4:p.Ser679Ter
ENST00000348990.9:c.1811C>G ENSP00000345463.5:p.Ser604Ter
ENST00000354192.7:c.1643C>G ENSP00000346129.3:p.Ser548Ter
ENST00000357903.7:c.1979C>G ENSP00000350578.3:p.Ser660Ter
ENST00000358918.7:c.1982C>G ENSP00000351796.3:p.Ser661Ter
ENST00000359726.7:c.1706C>G ENSP00000352760.4:p.Ser569Ter
ENST00000439274.6:c.1868C>G ENSP00000398879.2:p.Ser623Ter
ENST00000440126.7:c.1964C>G ENSP00000387483.2:p.Ser655Ter
ENST00000464867.1:n.383C>G
NM_000484.3:c.2036C>G NP_000475.1:p.Ser679Ter
NM_001136016.3:c.1964C>G NP_001129488.1:p.Ser655Ter
NM_001136129.2:c.1643C>G NP_001129601.1:p.Ser548Ter
NM_001136130.2:c.1868C>G NP_001129602.1:p.Ser623Ter
NM_001136131.2:c.1706C>G NP_001129603.1:p.Ser569Ter
NM_001204301.1:c.1982C>G NP_001191230.1:p.Ser661Ter
NM_001204302.1:c.1925C>G NP_001191231.1:p.Ser642Ter
NM_001204303.1:c.1757C>G NP_001191232.1:p.Ser586Ter
NM_201413.2:c.1979C>G NP_958816.1:p.Ser660Ter
NM_201414.2:c.1811C>G NP_958817.1:p.Ser604Ter
NM_000484.4:c.2036C>G MANE Select NP_000475.1:p.Ser679Ter
NM_001136129.3:c.1643C>G NP_001129601.1:p.Ser548Ter
NM_001136130.3:c.1868C>G NP_001129602.1:p.Ser623Ter
NM_001204301.2:c.1982C>G NP_001191230.1:p.Ser661Ter
NM_001204302.2:c.1925C>G NP_001191231.1:p.Ser642Ter
NM_001204303.2:c.1757C>G NP_001191232.1:p.Ser586Ter
NM_201413.3:c.1979C>G NP_958816.1:p.Ser660Ter
NM_201414.3:c.1811C>G NP_958817.1:p.Ser604Ter
NM_001136131.3:c.1706C>G NP_001129603.1:p.Ser569Ter
NM_001385253.1:c.1868C>G NP_001372182.1:p.Ser623Ter