Canonical Allele Identifier: CA2383551621

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891795G= , CM000683.2:g.25891795G=	GRCh38
NC_000021.8:g.27264107G= , CM000683.1:g.27264107G=	GRCh37
NC_000021.7:g.26185978G=	NCBI36
NG_007376.1:g.284026C=
NG_007376.2:g.284334C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2105C=
ENST00000707133.1:n.535C=
ENST00000707134.1:n.804C=
ENST00000346798.8:c.2138C= MANE Select	ENSP00000284981.4:p.Ala713=
ENST00000346798.7:c.2138C=	ENSP00000284981.4:p.Ala713=
ENST00000348990.9:c.1913C=	ENSP00000345463.5:p.Ala638=
ENST00000354192.7:c.1745C=	ENSP00000346129.3:p.Ala582=
ENST00000357903.7:c.2081C=	ENSP00000350578.3:p.Ala694=
ENST00000358918.7:c.2084C=	ENSP00000351796.3:p.Ala695=
ENST00000359726.7:c.1808C=	ENSP00000352760.4:p.Ala603=
ENST00000439274.6:c.1970C=	ENSP00000398879.2:p.Ala657=
ENST00000440126.7:c.2066C=	ENSP00000387483.2:p.Ala689=
ENST00000464867.1:n.485C=
NM_000484.3:c.2138C=	NP_000475.1:p.Ala713=
NM_001136016.3:c.2066C=	NP_001129488.1:p.Ala689=
NM_001136129.2:c.1745C=	NP_001129601.1:p.Ala582=
NM_001136130.2:c.1970C=	NP_001129602.1:p.Ala657=
NM_001136131.2:c.1808C=	NP_001129603.1:p.Ala603=
NM_001204301.1:c.2084C=	NP_001191230.1:p.Ala695=
NM_001204302.1:c.2027C=	NP_001191231.1:p.Ala676=
NM_001204303.1:c.1859C=	NP_001191232.1:p.Ala620=
NM_201413.2:c.2081C=	NP_958816.1:p.Ala694=
NM_201414.2:c.1913C=	NP_958817.1:p.Ala638=
NM_000484.4:c.2138C= MANE Select	NP_000475.1:p.Ala713=
NM_001136129.3:c.1745C=	NP_001129601.1:p.Ala582=
NM_001136130.3:c.1970C=	NP_001129602.1:p.Ala657=
NM_001204301.2:c.2084C=	NP_001191230.1:p.Ala695=
NM_001204302.2:c.2027C=	NP_001191231.1:p.Ala676=
NM_001204303.2:c.1859C=	NP_001191232.1:p.Ala620=
NM_201413.3:c.2081C=	NP_958816.1:p.Ala694=
NM_201414.3:c.1913C=	NP_958817.1:p.Ala638=
NM_001136131.3:c.1808C=	NP_001129603.1:p.Ala603=
NM_001385253.1:c.1970C=	NP_001372182.1:p.Ala657=