Canonical Allele Identifier: CA409805543
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891779G>C , CM000683.2:g.25891779G>C GRCh38
NC_000021.8:g.27264091G>C , CM000683.1:g.27264091G>C GRCh37
NC_000021.7:g.26185962G>C NCBI36
NG_007376.1:g.284042C>G
NG_007376.2:g.284350C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2154C>G MANE Select ENSP00000284981.4:p.Ile718Met
ENST00000346798.7:c.2154C>G ENSP00000284981.4:p.Ile718Met
ENST00000348990.9:c.1929C>G ENSP00000345463.5:p.Ile643Met
ENST00000354192.7:c.1761C>G ENSP00000346129.3:p.Ile587Met
ENST00000357903.7:c.2097C>G ENSP00000350578.3:p.Ile699Met
ENST00000358918.7:c.2100C>G ENSP00000351796.3:p.Ile700Met
ENST00000359726.7:c.1824C>G ENSP00000352760.4:p.Ile608Met
ENST00000439274.6:c.1986C>G ENSP00000398879.2:p.Ile662Met
ENST00000440126.7:c.2082C>G ENSP00000387483.2:p.Ile694Met
ENST00000464867.1:n.501C>G
NM_000484.3:c.2154C>G NP_000475.1:p.Ile718Met
NM_001136016.3:c.2082C>G NP_001129488.1:p.Ile694Met
NM_001136129.2:c.1761C>G NP_001129601.1:p.Ile587Met
NM_001136130.2:c.1986C>G NP_001129602.1:p.Ile662Met
NM_001136131.2:c.1824C>G NP_001129603.1:p.Ile608Met
NM_001204301.1:c.2100C>G NP_001191230.1:p.Ile700Met
NM_001204302.1:c.2043C>G NP_001191231.1:p.Ile681Met
NM_001204303.1:c.1875C>G NP_001191232.1:p.Ile625Met
NM_201413.2:c.2097C>G NP_958816.1:p.Ile699Met
NM_201414.2:c.1929C>G NP_958817.1:p.Ile643Met
NM_000484.4:c.2154C>G MANE Select NP_000475.1:p.Ile718Met
NM_001136129.3:c.1761C>G NP_001129601.1:p.Ile587Met
NM_001136130.3:c.1986C>G NP_001129602.1:p.Ile662Met
NM_001204301.2:c.2100C>G NP_001191230.1:p.Ile700Met
NM_001204302.2:c.2043C>G NP_001191231.1:p.Ile681Met
NM_001204303.2:c.1875C>G NP_001191232.1:p.Ile625Met
NM_201413.3:c.2097C>G NP_958816.1:p.Ile699Met
NM_201414.3:c.1929C>G NP_958817.1:p.Ile643Met
NM_001136131.3:c.1824C>G NP_001129603.1:p.Ile608Met
NM_001385253.1:c.1986C>G NP_001372182.1:p.Ile662Met