Canonical Allele Identifier: CA511685995
Gene: APP HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.27264094G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891782G>A , CM000683.2:g.25891782G>A GRCh38
NC_000021.8:g.27264094G>A , CM000683.1:g.27264094G>A GRCh37
NC_000021.7:g.26185965G>A NCBI36
NG_007376.1:g.284039C>T
NG_007376.2:g.284347C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2151C>T MANE Select ENSP00000284981.4:p.Val717=
ENST00000346798.7:c.2151C>T ENSP00000284981.4:p.Val717=
ENST00000348990.9:c.1926C>T ENSP00000345463.5:p.Val642=
ENST00000354192.7:c.1758C>T ENSP00000346129.3:p.Val586=
ENST00000357903.7:c.2094C>T ENSP00000350578.3:p.Val698=
ENST00000358918.7:c.2097C>T ENSP00000351796.3:p.Val699=
ENST00000359726.7:c.1821C>T ENSP00000352760.4:p.Val607=
ENST00000439274.6:c.1983C>T ENSP00000398879.2:p.Val661=
ENST00000440126.7:c.2079C>T ENSP00000387483.2:p.Val693=
ENST00000464867.1:n.498C>T
NM_000484.3:c.2151C>T NP_000475.1:p.Val717=
NM_001136016.3:c.2079C>T NP_001129488.1:p.Val693=
NM_001136129.2:c.1758C>T NP_001129601.1:p.Val586=
NM_001136130.2:c.1983C>T NP_001129602.1:p.Val661=
NM_001136131.2:c.1821C>T NP_001129603.1:p.Val607=
NM_001204301.1:c.2097C>T NP_001191230.1:p.Val699=
NM_001204302.1:c.2040C>T NP_001191231.1:p.Val680=
NM_001204303.1:c.1872C>T NP_001191232.1:p.Val624=
NM_201413.2:c.2094C>T NP_958816.1:p.Val698=
NM_201414.2:c.1926C>T NP_958817.1:p.Val642=
NM_000484.4:c.2151C>T MANE Select NP_000475.1:p.Val717=
NM_001136129.3:c.1758C>T NP_001129601.1:p.Val586=
NM_001136130.3:c.1983C>T NP_001129602.1:p.Val661=
NM_001204301.2:c.2097C>T NP_001191230.1:p.Val699=
NM_001204302.2:c.2040C>T NP_001191231.1:p.Val680=
NM_001204303.2:c.1872C>T NP_001191232.1:p.Val624=
NM_201413.3:c.2094C>T NP_958816.1:p.Val698=
NM_201414.3:c.1926C>T NP_958817.1:p.Val642=
NM_001136131.3:c.1821C>T NP_001129603.1:p.Val607=
NM_001385253.1:c.1983C>T NP_001372182.1:p.Val661=