Canonical Allele Identifier: CA511686004

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27264109T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891797T>A , CM000683.2:g.25891797T>A	GRCh38
NC_000021.8:g.27264109T>A , CM000683.1:g.27264109T>A	GRCh37
NC_000021.7:g.26185980T>A	NCBI36
NG_007376.1:g.284024A>T
NG_007376.2:g.284332A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2103A>T
ENST00000707133.1:n.533A>T
ENST00000707134.1:n.802A>T
ENST00000346798.8:c.2136A>T MANE Select	ENSP00000284981.4:p.Ile712=
ENST00000346798.7:c.2136A>T	ENSP00000284981.4:p.Ile712=
ENST00000348990.9:c.1911A>T	ENSP00000345463.5:p.Ile637=
ENST00000354192.7:c.1743A>T	ENSP00000346129.3:p.Ile581=
ENST00000357903.7:c.2079A>T	ENSP00000350578.3:p.Ile693=
ENST00000358918.7:c.2082A>T	ENSP00000351796.3:p.Ile694=
ENST00000359726.7:c.1806A>T	ENSP00000352760.4:p.Ile602=
ENST00000439274.6:c.1968A>T	ENSP00000398879.2:p.Ile656=
ENST00000440126.7:c.2064A>T	ENSP00000387483.2:p.Ile688=
ENST00000464867.1:n.483A>T
NM_000484.3:c.2136A>T	NP_000475.1:p.Ile712=
NM_001136016.3:c.2064A>T	NP_001129488.1:p.Ile688=
NM_001136129.2:c.1743A>T	NP_001129601.1:p.Ile581=
NM_001136130.2:c.1968A>T	NP_001129602.1:p.Ile656=
NM_001136131.2:c.1806A>T	NP_001129603.1:p.Ile602=
NM_001204301.1:c.2082A>T	NP_001191230.1:p.Ile694=
NM_001204302.1:c.2025A>T	NP_001191231.1:p.Ile675=
NM_001204303.1:c.1857A>T	NP_001191232.1:p.Ile619=
NM_201413.2:c.2079A>T	NP_958816.1:p.Ile693=
NM_201414.2:c.1911A>T	NP_958817.1:p.Ile637=
NM_000484.4:c.2136A>T MANE Select	NP_000475.1:p.Ile712=
NM_001136129.3:c.1743A>T	NP_001129601.1:p.Ile581=
NM_001136130.3:c.1968A>T	NP_001129602.1:p.Ile656=
NM_001204301.2:c.2082A>T	NP_001191230.1:p.Ile694=
NM_001204302.2:c.2025A>T	NP_001191231.1:p.Ile675=
NM_001204303.2:c.1857A>T	NP_001191232.1:p.Ile619=
NM_201413.3:c.2079A>T	NP_958816.1:p.Ile693=
NM_201414.3:c.1911A>T	NP_958817.1:p.Ile637=
NM_001136131.3:c.1806A>T	NP_001129603.1:p.Ile602=
NM_001385253.1:c.1968A>T	NP_001372182.1:p.Ile656=