Canonical Allele Identifier: CA409805526
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891771A>T , CM000683.2:g.25891771A>T GRCh38
NC_000021.8:g.27264083A>T , CM000683.1:g.27264083A>T GRCh37
NC_000021.7:g.26185954A>T NCBI36
NG_007376.1:g.284050T>A
NG_007376.2:g.284358T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2162T>A MANE Select ENSP00000284981.4:p.Val721Glu
ENST00000346798.7:c.2162T>A ENSP00000284981.4:p.Val721Glu
ENST00000348990.9:c.1937T>A ENSP00000345463.5:p.Val646Glu
ENST00000354192.7:c.1769T>A ENSP00000346129.3:p.Val590Glu
ENST00000357903.7:c.2105T>A ENSP00000350578.3:p.Val702Glu
ENST00000358918.7:c.2108T>A ENSP00000351796.3:p.Val703Glu
ENST00000359726.7:c.1832T>A ENSP00000352760.4:p.Val611Glu
ENST00000439274.6:c.1994T>A ENSP00000398879.2:p.Val665Glu
ENST00000440126.7:c.2090T>A ENSP00000387483.2:p.Val697Glu
ENST00000464867.1:n.509T>A
NM_000484.3:c.2162T>A NP_000475.1:p.Val721Glu
NM_001136016.3:c.2090T>A NP_001129488.1:p.Val697Glu
NM_001136129.2:c.1769T>A NP_001129601.1:p.Val590Glu
NM_001136130.2:c.1994T>A NP_001129602.1:p.Val665Glu
NM_001136131.2:c.1832T>A NP_001129603.1:p.Val611Glu
NM_001204301.1:c.2108T>A NP_001191230.1:p.Val703Glu
NM_001204302.1:c.2051T>A NP_001191231.1:p.Val684Glu
NM_001204303.1:c.1883T>A NP_001191232.1:p.Val628Glu
NM_201413.2:c.2105T>A NP_958816.1:p.Val702Glu
NM_201414.2:c.1937T>A NP_958817.1:p.Val646Glu
NM_000484.4:c.2162T>A MANE Select NP_000475.1:p.Val721Glu
NM_001136129.3:c.1769T>A NP_001129601.1:p.Val590Glu
NM_001136130.3:c.1994T>A NP_001129602.1:p.Val665Glu
NM_001204301.2:c.2108T>A NP_001191230.1:p.Val703Glu
NM_001204302.2:c.2051T>A NP_001191231.1:p.Val684Glu
NM_001204303.2:c.1883T>A NP_001191232.1:p.Val628Glu
NM_201413.3:c.2105T>A NP_958816.1:p.Val702Glu
NM_201414.3:c.1937T>A NP_958817.1:p.Val646Glu
NM_001136131.3:c.1832T>A NP_001129603.1:p.Val611Glu
NM_001385253.1:c.1994T>A NP_001372182.1:p.Val665Glu