Canonical Allele Identifier: CA409806244
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897580T>G , CM000683.2:g.25897580T>G GRCh38
NC_000021.8:g.27269892T>G , CM000683.1:g.27269892T>G GRCh37
NC_000021.7:g.26191763T>G NCBI36
NG_007376.1:g.278241A>C
NG_007376.2:g.278549A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2024A>C
ENST00000707133.1:n.454A>C
ENST00000707134.1:n.723A>C
ENST00000346798.8:c.2057A>C MANE Select ENSP00000284981.4:p.Gln686Pro
ENST00000346798.7:c.2057A>C ENSP00000284981.4:p.Gln686Pro
ENST00000348990.9:c.1832A>C ENSP00000345463.5:p.Gln611Pro
ENST00000354192.7:c.1664A>C ENSP00000346129.3:p.Gln555Pro
ENST00000357903.7:c.2000A>C ENSP00000350578.3:p.Gln667Pro
ENST00000358918.7:c.2003A>C ENSP00000351796.3:p.Gln668Pro
ENST00000359726.7:c.1727A>C ENSP00000352760.4:p.Gln576Pro
ENST00000439274.6:c.1889A>C ENSP00000398879.2:p.Gln630Pro
ENST00000440126.7:c.1985A>C ENSP00000387483.2:p.Gln662Pro
ENST00000464867.1:n.404A>C
NM_000484.3:c.2057A>C NP_000475.1:p.Gln686Pro
NM_001136016.3:c.1985A>C NP_001129488.1:p.Gln662Pro
NM_001136129.2:c.1664A>C NP_001129601.1:p.Gln555Pro
NM_001136130.2:c.1889A>C NP_001129602.1:p.Gln630Pro
NM_001136131.2:c.1727A>C NP_001129603.1:p.Gln576Pro
NM_001204301.1:c.2003A>C NP_001191230.1:p.Gln668Pro
NM_001204302.1:c.1946A>C NP_001191231.1:p.Gln649Pro
NM_001204303.1:c.1778A>C NP_001191232.1:p.Gln593Pro
NM_201413.2:c.2000A>C NP_958816.1:p.Gln667Pro
NM_201414.2:c.1832A>C NP_958817.1:p.Gln611Pro
NM_000484.4:c.2057A>C MANE Select NP_000475.1:p.Gln686Pro
NM_001136129.3:c.1664A>C NP_001129601.1:p.Gln555Pro
NM_001136130.3:c.1889A>C NP_001129602.1:p.Gln630Pro
NM_001204301.2:c.2003A>C NP_001191230.1:p.Gln668Pro
NM_001204302.2:c.1946A>C NP_001191231.1:p.Gln649Pro
NM_001204303.2:c.1778A>C NP_001191232.1:p.Gln593Pro
NM_201413.3:c.2000A>C NP_958816.1:p.Gln667Pro
NM_201414.3:c.1832A>C NP_958817.1:p.Gln611Pro
NM_001136131.3:c.1727A>C NP_001129603.1:p.Gln576Pro
NM_001385253.1:c.1889A>C NP_001372182.1:p.Gln630Pro