Canonical Allele Identifier: CA409806340
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897602A>C , CM000683.2:g.25897602A>C GRCh38
NC_000021.8:g.27269914A>C , CM000683.1:g.27269914A>C GRCh37
NC_000021.7:g.26191785A>C NCBI36
NG_007376.1:g.278219T>G
NG_007376.2:g.278527T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2002T>G
ENST00000707133.1:n.432T>G
ENST00000707134.1:n.701T>G
ENST00000346798.8:c.2035T>G MANE Select ENSP00000284981.4:p.Ser679Ala
ENST00000346798.7:c.2035T>G ENSP00000284981.4:p.Ser679Ala
ENST00000348990.9:c.1810T>G ENSP00000345463.5:p.Ser604Ala
ENST00000354192.7:c.1642T>G ENSP00000346129.3:p.Ser548Ala
ENST00000357903.7:c.1978T>G ENSP00000350578.3:p.Ser660Ala
ENST00000358918.7:c.1981T>G ENSP00000351796.3:p.Ser661Ala
ENST00000359726.7:c.1705T>G ENSP00000352760.4:p.Ser569Ala
ENST00000439274.6:c.1867T>G ENSP00000398879.2:p.Ser623Ala
ENST00000440126.7:c.1963T>G ENSP00000387483.2:p.Ser655Ala
ENST00000464867.1:n.382T>G
NM_000484.3:c.2035T>G NP_000475.1:p.Ser679Ala
NM_001136016.3:c.1963T>G NP_001129488.1:p.Ser655Ala
NM_001136129.2:c.1642T>G NP_001129601.1:p.Ser548Ala
NM_001136130.2:c.1867T>G NP_001129602.1:p.Ser623Ala
NM_001136131.2:c.1705T>G NP_001129603.1:p.Ser569Ala
NM_001204301.1:c.1981T>G NP_001191230.1:p.Ser661Ala
NM_001204302.1:c.1924T>G NP_001191231.1:p.Ser642Ala
NM_001204303.1:c.1756T>G NP_001191232.1:p.Ser586Ala
NM_201413.2:c.1978T>G NP_958816.1:p.Ser660Ala
NM_201414.2:c.1810T>G NP_958817.1:p.Ser604Ala
NM_000484.4:c.2035T>G MANE Select NP_000475.1:p.Ser679Ala
NM_001136129.3:c.1642T>G NP_001129601.1:p.Ser548Ala
NM_001136130.3:c.1867T>G NP_001129602.1:p.Ser623Ala
NM_001204301.2:c.1981T>G NP_001191230.1:p.Ser661Ala
NM_001204302.2:c.1924T>G NP_001191231.1:p.Ser642Ala
NM_001204303.2:c.1756T>G NP_001191232.1:p.Ser586Ala
NM_201413.3:c.1978T>G NP_958816.1:p.Ser660Ala
NM_201414.3:c.1810T>G NP_958817.1:p.Ser604Ala
NM_001136131.3:c.1705T>G NP_001129603.1:p.Ser569Ala
NM_001385253.1:c.1867T>G NP_001372182.1:p.Ser623Ala