Canonical Allele Identifier: CA2383554900

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897575A= , CM000683.2:g.25897575A=	GRCh38
NC_000021.8:g.27269887A= , CM000683.1:g.27269887A=	GRCh37
NC_000021.7:g.26191758A=	NCBI36
NG_007376.1:g.278246T=
NG_007376.2:g.278554T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2029T=
ENST00000707133.1:n.459T=
ENST00000707134.1:n.728T=
ENST00000346798.8:c.2062T= MANE Select	ENSP00000284981.4:p.Leu688=
ENST00000346798.7:c.2062T=	ENSP00000284981.4:p.Leu688=
ENST00000348990.9:c.1837T=	ENSP00000345463.5:p.Leu613=
ENST00000354192.7:c.1669T=	ENSP00000346129.3:p.Leu557=
ENST00000357903.7:c.2005T=	ENSP00000350578.3:p.Leu669=
ENST00000358918.7:c.2008T=	ENSP00000351796.3:p.Leu670=
ENST00000359726.7:c.1732T=	ENSP00000352760.4:p.Leu578=
ENST00000439274.6:c.1894T=	ENSP00000398879.2:p.Leu632=
ENST00000440126.7:c.1990T=	ENSP00000387483.2:p.Leu664=
ENST00000464867.1:n.409T=
NM_000484.3:c.2062T=	NP_000475.1:p.Leu688=
NM_001136016.3:c.1990T=	NP_001129488.1:p.Leu664=
NM_001136129.2:c.1669T=	NP_001129601.1:p.Leu557=
NM_001136130.2:c.1894T=	NP_001129602.1:p.Leu632=
NM_001136131.2:c.1732T=	NP_001129603.1:p.Leu578=
NM_001204301.1:c.2008T=	NP_001191230.1:p.Leu670=
NM_001204302.1:c.1951T=	NP_001191231.1:p.Leu651=
NM_001204303.1:c.1783T=	NP_001191232.1:p.Leu595=
NM_201413.2:c.2005T=	NP_958816.1:p.Leu669=
NM_201414.2:c.1837T=	NP_958817.1:p.Leu613=
NM_000484.4:c.2062T= MANE Select	NP_000475.1:p.Leu688=
NM_001136129.3:c.1669T=	NP_001129601.1:p.Leu557=
NM_001136130.3:c.1894T=	NP_001129602.1:p.Leu632=
NM_001204301.2:c.2008T=	NP_001191230.1:p.Leu670=
NM_001204302.2:c.1951T=	NP_001191231.1:p.Leu651=
NM_001204303.2:c.1783T=	NP_001191232.1:p.Leu595=
NM_201413.3:c.2005T=	NP_958816.1:p.Leu669=
NM_201414.3:c.1837T=	NP_958817.1:p.Leu613=
NM_001136131.3:c.1732T=	NP_001129603.1:p.Leu578=
NM_001385253.1:c.1894T=	NP_001372182.1:p.Leu632=