Canonical Allele Identifier: CA2383554944

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897649G= , CM000683.2:g.25897649G=	GRCh38
NC_000021.8:g.27269961G= , CM000683.1:g.27269961G=	GRCh37
NC_000021.7:g.26191832G=	NCBI36
NG_007376.1:g.278172C=
NG_007376.2:g.278480C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.1955C=
ENST00000707133.1:n.385C=
ENST00000707134.1:n.654C=
ENST00000346798.8:c.1988C= MANE Select	ENSP00000284981.4:p.Thr663=
ENST00000346798.7:c.1988C=	ENSP00000284981.4:p.Thr663=
ENST00000348990.9:c.1763C=	ENSP00000345463.5:p.Thr588=
ENST00000354192.7:c.1595C=	ENSP00000346129.3:p.Thr532=
ENST00000357903.7:c.1931C=	ENSP00000350578.3:p.Thr644=
ENST00000358918.7:c.1934C=	ENSP00000351796.3:p.Thr645=
ENST00000359726.7:c.1658C=	ENSP00000352760.4:p.Thr553=
ENST00000439274.6:c.1820C=	ENSP00000398879.2:p.Thr607=
ENST00000440126.7:c.1916C=	ENSP00000387483.2:p.Thr639=
ENST00000464867.1:n.335C=
NM_000484.3:c.1988C=	NP_000475.1:p.Thr663=
NM_001136016.3:c.1916C=	NP_001129488.1:p.Thr639=
NM_001136129.2:c.1595C=	NP_001129601.1:p.Thr532=
NM_001136130.2:c.1820C=	NP_001129602.1:p.Thr607=
NM_001136131.2:c.1658C=	NP_001129603.1:p.Thr553=
NM_001204301.1:c.1934C=	NP_001191230.1:p.Thr645=
NM_001204302.1:c.1877C=	NP_001191231.1:p.Thr626=
NM_001204303.1:c.1709C=	NP_001191232.1:p.Thr570=
NM_201413.2:c.1931C=	NP_958816.1:p.Thr644=
NM_201414.2:c.1763C=	NP_958817.1:p.Thr588=
NM_000484.4:c.1988C= MANE Select	NP_000475.1:p.Thr663=
NM_001136129.3:c.1595C=	NP_001129601.1:p.Thr532=
NM_001136130.3:c.1820C=	NP_001129602.1:p.Thr607=
NM_001204301.2:c.1934C=	NP_001191230.1:p.Thr645=
NM_001204302.2:c.1877C=	NP_001191231.1:p.Thr626=
NM_001204303.2:c.1709C=	NP_001191232.1:p.Thr570=
NM_201413.3:c.1931C=	NP_958816.1:p.Thr644=
NM_201414.3:c.1763C=	NP_958817.1:p.Thr588=
NM_001136131.3:c.1658C=	NP_001129603.1:p.Thr553=
NM_001385253.1:c.1820C=	NP_001372182.1:p.Thr607=