Canonical Allele Identifier: CA2383551628

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891808C= , CM000683.2:g.25891808C=	GRCh38
NC_000021.8:g.27264120C= , CM000683.1:g.27264120C=	GRCh37
NC_000021.7:g.26185991C=	NCBI36
NG_007376.1:g.284013G=
NG_007376.2:g.284321G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2092G=
ENST00000707133.1:n.522G=
ENST00000707134.1:n.791G=
ENST00000346798.8:c.2125G= MANE Select	ENSP00000284981.4:p.Gly709=
ENST00000346798.7:c.2125G=	ENSP00000284981.4:p.Gly709=
ENST00000348990.9:c.1900G=	ENSP00000345463.5:p.Gly634=
ENST00000354192.7:c.1732G=	ENSP00000346129.3:p.Gly578=
ENST00000357903.7:c.2068G=	ENSP00000350578.3:p.Gly690=
ENST00000358918.7:c.2071G=	ENSP00000351796.3:p.Gly691=
ENST00000359726.7:c.1795G=	ENSP00000352760.4:p.Gly599=
ENST00000439274.6:c.1957G=	ENSP00000398879.2:p.Gly653=
ENST00000440126.7:c.2053G=	ENSP00000387483.2:p.Gly685=
ENST00000464867.1:n.472G=
NM_000484.3:c.2125G=	NP_000475.1:p.Gly709=
NM_001136016.3:c.2053G=	NP_001129488.1:p.Gly685=
NM_001136129.2:c.1732G=	NP_001129601.1:p.Gly578=
NM_001136130.2:c.1957G=	NP_001129602.1:p.Gly653=
NM_001136131.2:c.1795G=	NP_001129603.1:p.Gly599=
NM_001204301.1:c.2071G=	NP_001191230.1:p.Gly691=
NM_001204302.1:c.2014G=	NP_001191231.1:p.Gly672=
NM_001204303.1:c.1846G=	NP_001191232.1:p.Gly616=
NM_201413.2:c.2068G=	NP_958816.1:p.Gly690=
NM_201414.2:c.1900G=	NP_958817.1:p.Gly634=
NM_000484.4:c.2125G= MANE Select	NP_000475.1:p.Gly709=
NM_001136129.3:c.1732G=	NP_001129601.1:p.Gly578=
NM_001136130.3:c.1957G=	NP_001129602.1:p.Gly653=
NM_001204301.2:c.2071G=	NP_001191230.1:p.Gly691=
NM_001204302.2:c.2014G=	NP_001191231.1:p.Gly672=
NM_001204303.2:c.1846G=	NP_001191232.1:p.Gly616=
NM_201413.3:c.2068G=	NP_958816.1:p.Gly690=
NM_201414.3:c.1900G=	NP_958817.1:p.Gly634=
NM_001136131.3:c.1795G=	NP_001129603.1:p.Gly599=
NM_001385253.1:c.1957G=	NP_001372182.1:p.Gly653=