Canonical Allele Identifier: CA409805520
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891768A>C , CM000683.2:g.25891768A>C GRCh38
NC_000021.8:g.27264080A>C , CM000683.1:g.27264080A>C GRCh37
NC_000021.7:g.26185951A>C NCBI36
NG_007376.1:g.284053T>G
NG_007376.2:g.284361T>G

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2165T>G NP_000475.1:p.Met722Arg
NM_001136016.3:c.2093T>G NP_001129488.1:p.Met698Arg
NM_001136129.2:c.1772T>G NP_001129601.1:p.Met591Arg
NM_001136130.2:c.1997T>G NP_001129602.1:p.Met666Arg
NM_001136131.2:c.1835T>G NP_001129603.1:p.Met612Arg
NM_001204301.1:c.2111T>G NP_001191230.1:p.Met704Arg
NM_001204302.1:c.2054T>G NP_001191231.1:p.Met685Arg
NM_001204303.1:c.1886T>G NP_001191232.1:p.Met629Arg
NM_201413.2:c.2108T>G NP_958816.1:p.Met703Arg
NM_201414.2:c.1940T>G NP_958817.1:p.Met647Arg
NM_000484.4:c.2165T>G MANE Select NP_000475.1:p.Met722Arg
NM_001136129.3:c.1772T>G NP_001129601.1:p.Met591Arg
NM_001136130.3:c.1997T>G NP_001129602.1:p.Met666Arg
NM_001204301.2:c.2111T>G NP_001191230.1:p.Met704Arg
NM_001204302.2:c.2054T>G NP_001191231.1:p.Met685Arg
NM_001204303.2:c.1886T>G NP_001191232.1:p.Met629Arg
NM_201413.3:c.2108T>G NP_958816.1:p.Met703Arg
NM_201414.3:c.1940T>G NP_958817.1:p.Met647Arg
NM_001136131.3:c.1835T>G NP_001129603.1:p.Met612Arg
NM_001385253.1:c.1997T>G NP_001372182.1:p.Met666Arg
ENST00000346798.7:c.2165T>G ENSP00000284981.4:p.Met722Arg
ENST00000348990.9:c.1940T>G ENSP00000345463.5:p.Met647Arg
ENST00000354192.7:c.1772T>G ENSP00000346129.3:p.Met591Arg
ENST00000357903.7:c.2108T>G ENSP00000350578.3:p.Met703Arg
ENST00000358918.7:c.2111T>G ENSP00000351796.3:p.Met704Arg
ENST00000359726.7:c.1835T>G ENSP00000352760.4:p.Met612Arg
ENST00000439274.6:c.1997T>G ENSP00000398879.2:p.Met666Arg
ENST00000440126.7:c.2093T>G ENSP00000387483.2:p.Met698Arg
ENST00000464867.1:n.512T>G