Canonical Allele Identifier: CA3243796648

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891774A= , CM000683.2:g.25891774A=	GRCh38
NC_000021.8:g.27264086A= , CM000683.1:g.27264086A=	GRCh37
NC_000021.7:g.26185957A=	NCBI36
NG_007376.1:g.284047T=
NG_007376.2:g.284355T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000484.4:c.2159T= MANE Select	NP_000475.1:p.Leu720=
ENST00000346798.8:c.2159T= MANE Select	ENSP00000284981.4:p.Leu720=
NM_000484.3:c.2159T=	NP_000475.1:p.Leu720=
NM_001136016.3:c.2087T=	NP_001129488.1:p.Leu696=
NM_001136129.2:c.1766T=	NP_001129601.1:p.Leu589=
NM_001136129.3:c.1766T=	NP_001129601.1:p.Leu589=
NM_001136130.2:c.1991T=	NP_001129602.1:p.Leu664=
NM_001136130.3:c.1991T=	NP_001129602.1:p.Leu664=
NM_001136131.2:c.1829T=	NP_001129603.1:p.Leu610=
NM_001136131.3:c.1829T=	NP_001129603.1:p.Leu610=
NM_001204301.1:c.2105T=	NP_001191230.1:p.Leu702=
NM_001204301.2:c.2105T=	NP_001191230.1:p.Leu702=
NM_001204302.1:c.2048T=	NP_001191231.1:p.Leu683=
NM_001204302.2:c.2048T=	NP_001191231.1:p.Leu683=
NM_001204303.1:c.1880T=	NP_001191232.1:p.Leu627=
NM_001204303.2:c.1880T=	NP_001191232.1:p.Leu627=
NM_001385253.1:c.1991T=	NP_001372182.1:p.Leu664=
NM_201413.2:c.2102T=	NP_958816.1:p.Leu701=
NM_201413.3:c.2102T=	NP_958816.1:p.Leu701=
NM_201414.2:c.1934T=	NP_958817.1:p.Leu645=
NM_201414.3:c.1934T=	NP_958817.1:p.Leu645=
ENST00000346798.7:c.2159T=	ENSP00000284981.4:p.Leu720=
ENST00000348990.9:c.1934T=	ENSP00000345463.5:p.Leu645=
ENST00000354192.7:c.1766T=	ENSP00000346129.3:p.Leu589=
ENST00000357903.7:c.2102T=	ENSP00000350578.3:p.Leu701=
ENST00000358918.7:c.2105T=	ENSP00000351796.3:p.Leu702=
ENST00000359726.7:c.1829T=	ENSP00000352760.4:p.Leu610=
ENST00000439274.6:c.1991T=	ENSP00000398879.2:p.Leu664=
ENST00000440126.7:c.2087T=	ENSP00000387483.2:p.Leu696=
ENST00000464867.1:n.506T=
ENST00000707132.1:n.2126T=
ENST00000707133.1:n.556T=
ENST00000707134.1:n.825T=