Canonical Allele Identifier: CA409806521
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897643T>G , CM000683.2:g.25897643T>G GRCh38
NC_000021.8:g.27269955T>G , CM000683.1:g.27269955T>G GRCh37
NC_000021.7:g.26191826T>G NCBI36
NG_007376.1:g.278178A>C
NG_007376.2:g.278486A>C

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.1994A>C NP_000475.1:p.Glu665Ala
NM_001136016.3:c.1922A>C NP_001129488.1:p.Glu641Ala
NM_001136129.2:c.1601A>C NP_001129601.1:p.Glu534Ala
NM_001136130.2:c.1826A>C NP_001129602.1:p.Glu609Ala
NM_001136131.2:c.1664A>C NP_001129603.1:p.Glu555Ala
NM_001204301.1:c.1940A>C NP_001191230.1:p.Glu647Ala
NM_001204302.1:c.1883A>C NP_001191231.1:p.Glu628Ala
NM_001204303.1:c.1715A>C NP_001191232.1:p.Glu572Ala
NM_201413.2:c.1937A>C NP_958816.1:p.Glu646Ala
NM_201414.2:c.1769A>C NP_958817.1:p.Glu590Ala
NM_000484.4:c.1994A>C MANE Select NP_000475.1:p.Glu665Ala
NM_001136129.3:c.1601A>C NP_001129601.1:p.Glu534Ala
NM_001136130.3:c.1826A>C NP_001129602.1:p.Glu609Ala
NM_001204301.2:c.1940A>C NP_001191230.1:p.Glu647Ala
NM_001204302.2:c.1883A>C NP_001191231.1:p.Glu628Ala
NM_001204303.2:c.1715A>C NP_001191232.1:p.Glu572Ala
NM_201413.3:c.1937A>C NP_958816.1:p.Glu646Ala
NM_201414.3:c.1769A>C NP_958817.1:p.Glu590Ala
NM_001136131.3:c.1664A>C NP_001129603.1:p.Glu555Ala
NM_001385253.1:c.1826A>C NP_001372182.1:p.Glu609Ala
ENST00000346798.7:c.1994A>C ENSP00000284981.4:p.Glu665Ala
ENST00000348990.9:c.1769A>C ENSP00000345463.5:p.Glu590Ala
ENST00000354192.7:c.1601A>C ENSP00000346129.3:p.Glu534Ala
ENST00000357903.7:c.1937A>C ENSP00000350578.3:p.Glu646Ala
ENST00000358918.7:c.1940A>C ENSP00000351796.3:p.Glu647Ala
ENST00000359726.7:c.1664A>C ENSP00000352760.4:p.Glu555Ala
ENST00000439274.6:c.1826A>C ENSP00000398879.2:p.Glu609Ala
ENST00000440126.7:c.1922A>C ENSP00000387483.2:p.Glu641Ala
ENST00000464867.1:n.341A>C