Canonical Allele Identifier: CA409806319
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897596A>G , CM000683.2:g.25897596A>G GRCh38
NC_000021.8:g.27269908A>G , CM000683.1:g.27269908A>G GRCh37
NC_000021.7:g.26191779A>G NCBI36
NG_007376.1:g.278225T>C
NG_007376.2:g.278533T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2008T>C
ENST00000707133.1:n.438T>C
ENST00000707134.1:n.707T>C
ENST00000346798.8:c.2041T>C MANE Select ENSP00000284981.4:p.Tyr681His
ENST00000346798.7:c.2041T>C ENSP00000284981.4:p.Tyr681His
ENST00000348990.9:c.1816T>C ENSP00000345463.5:p.Tyr606His
ENST00000354192.7:c.1648T>C ENSP00000346129.3:p.Tyr550His
ENST00000357903.7:c.1984T>C ENSP00000350578.3:p.Tyr662His
ENST00000358918.7:c.1987T>C ENSP00000351796.3:p.Tyr663His
ENST00000359726.7:c.1711T>C ENSP00000352760.4:p.Tyr571His
ENST00000439274.6:c.1873T>C ENSP00000398879.2:p.Tyr625His
ENST00000440126.7:c.1969T>C ENSP00000387483.2:p.Tyr657His
ENST00000464867.1:n.388T>C
NM_000484.3:c.2041T>C NP_000475.1:p.Tyr681His
NM_001136016.3:c.1969T>C NP_001129488.1:p.Tyr657His
NM_001136129.2:c.1648T>C NP_001129601.1:p.Tyr550His
NM_001136130.2:c.1873T>C NP_001129602.1:p.Tyr625His
NM_001136131.2:c.1711T>C NP_001129603.1:p.Tyr571His
NM_001204301.1:c.1987T>C NP_001191230.1:p.Tyr663His
NM_001204302.1:c.1930T>C NP_001191231.1:p.Tyr644His
NM_001204303.1:c.1762T>C NP_001191232.1:p.Tyr588His
NM_201413.2:c.1984T>C NP_958816.1:p.Tyr662His
NM_201414.2:c.1816T>C NP_958817.1:p.Tyr606His
NM_000484.4:c.2041T>C MANE Select NP_000475.1:p.Tyr681His
NM_001136129.3:c.1648T>C NP_001129601.1:p.Tyr550His
NM_001136130.3:c.1873T>C NP_001129602.1:p.Tyr625His
NM_001204301.2:c.1987T>C NP_001191230.1:p.Tyr663His
NM_001204302.2:c.1930T>C NP_001191231.1:p.Tyr644His
NM_001204303.2:c.1762T>C NP_001191232.1:p.Tyr588His
NM_201413.3:c.1984T>C NP_958816.1:p.Tyr662His
NM_201414.3:c.1816T>C NP_958817.1:p.Tyr606His
NM_001136131.3:c.1711T>C NP_001129603.1:p.Tyr571His
NM_001385253.1:c.1873T>C NP_001372182.1:p.Tyr625His