Canonical Allele Identifier: CA409805538
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891777G>C , CM000683.2:g.25891777G>C GRCh38
NC_000021.8:g.27264089G>C , CM000683.1:g.27264089G>C GRCh37
NC_000021.7:g.26185960G>C NCBI36
NG_007376.1:g.284044C>G
NG_007376.2:g.284352C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2156C>G MANE Select ENSP00000284981.4:p.Thr719Ser
ENST00000346798.7:c.2156C>G ENSP00000284981.4:p.Thr719Ser
ENST00000348990.9:c.1931C>G ENSP00000345463.5:p.Thr644Ser
ENST00000354192.7:c.1763C>G ENSP00000346129.3:p.Thr588Ser
ENST00000357903.7:c.2099C>G ENSP00000350578.3:p.Thr700Ser
ENST00000358918.7:c.2102C>G ENSP00000351796.3:p.Thr701Ser
ENST00000359726.7:c.1826C>G ENSP00000352760.4:p.Thr609Ser
ENST00000439274.6:c.1988C>G ENSP00000398879.2:p.Thr663Ser
ENST00000440126.7:c.2084C>G ENSP00000387483.2:p.Thr695Ser
ENST00000464867.1:n.503C>G
NM_000484.3:c.2156C>G NP_000475.1:p.Thr719Ser
NM_001136016.3:c.2084C>G NP_001129488.1:p.Thr695Ser
NM_001136129.2:c.1763C>G NP_001129601.1:p.Thr588Ser
NM_001136130.2:c.1988C>G NP_001129602.1:p.Thr663Ser
NM_001136131.2:c.1826C>G NP_001129603.1:p.Thr609Ser
NM_001204301.1:c.2102C>G NP_001191230.1:p.Thr701Ser
NM_001204302.1:c.2045C>G NP_001191231.1:p.Thr682Ser
NM_001204303.1:c.1877C>G NP_001191232.1:p.Thr626Ser
NM_201413.2:c.2099C>G NP_958816.1:p.Thr700Ser
NM_201414.2:c.1931C>G NP_958817.1:p.Thr644Ser
NM_000484.4:c.2156C>G MANE Select NP_000475.1:p.Thr719Ser
NM_001136129.3:c.1763C>G NP_001129601.1:p.Thr588Ser
NM_001136130.3:c.1988C>G NP_001129602.1:p.Thr663Ser
NM_001204301.2:c.2102C>G NP_001191230.1:p.Thr701Ser
NM_001204302.2:c.2045C>G NP_001191231.1:p.Thr682Ser
NM_001204303.2:c.1877C>G NP_001191232.1:p.Thr626Ser
NM_201413.3:c.2099C>G NP_958816.1:p.Thr700Ser
NM_201414.3:c.1931C>G NP_958817.1:p.Thr644Ser
NM_001136131.3:c.1826C>G NP_001129603.1:p.Thr609Ser
NM_001385253.1:c.1988C>G NP_001372182.1:p.Thr663Ser