Canonical Allele Identifier: CA2383554938

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897640A= , CM000683.2:g.25897640A=	GRCh38
NC_000021.8:g.27269952A= , CM000683.1:g.27269952A=	GRCh37
NC_000021.7:g.26191823A=	NCBI36
NG_007376.1:g.278181T=
NG_007376.2:g.278489T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1964T=
ENST00000707133.1:n.394T=
ENST00000707134.1:n.663T=
ENST00000346798.8:c.1997T= MANE Select	ENSP00000284981.4:p.Ile666=
ENST00000346798.7:c.1997T=	ENSP00000284981.4:p.Ile666=
ENST00000348990.9:c.1772T=	ENSP00000345463.5:p.Ile591=
ENST00000354192.7:c.1604T=	ENSP00000346129.3:p.Ile535=
ENST00000357903.7:c.1940T=	ENSP00000350578.3:p.Ile647=
ENST00000358918.7:c.1943T=	ENSP00000351796.3:p.Ile648=
ENST00000359726.7:c.1667T=	ENSP00000352760.4:p.Ile556=
ENST00000439274.6:c.1829T=	ENSP00000398879.2:p.Ile610=
ENST00000440126.7:c.1925T=	ENSP00000387483.2:p.Ile642=
ENST00000464867.1:n.344T=
NM_000484.3:c.1997T=	NP_000475.1:p.Ile666=
NM_001136016.3:c.1925T=	NP_001129488.1:p.Ile642=
NM_001136129.2:c.1604T=	NP_001129601.1:p.Ile535=
NM_001136130.2:c.1829T=	NP_001129602.1:p.Ile610=
NM_001136131.2:c.1667T=	NP_001129603.1:p.Ile556=
NM_001204301.1:c.1943T=	NP_001191230.1:p.Ile648=
NM_001204302.1:c.1886T=	NP_001191231.1:p.Ile629=
NM_001204303.1:c.1718T=	NP_001191232.1:p.Ile573=
NM_201413.2:c.1940T=	NP_958816.1:p.Ile647=
NM_201414.2:c.1772T=	NP_958817.1:p.Ile591=
NM_000484.4:c.1997T= MANE Select	NP_000475.1:p.Ile666=
NM_001136129.3:c.1604T=	NP_001129601.1:p.Ile535=
NM_001136130.3:c.1829T=	NP_001129602.1:p.Ile610=
NM_001204301.2:c.1943T=	NP_001191230.1:p.Ile648=
NM_001204302.2:c.1886T=	NP_001191231.1:p.Ile629=
NM_001204303.2:c.1718T=	NP_001191232.1:p.Ile573=
NM_201413.3:c.1940T=	NP_958816.1:p.Ile647=
NM_201414.3:c.1772T=	NP_958817.1:p.Ile591=
NM_001136131.3:c.1667T=	NP_001129603.1:p.Ile556=
NM_001385253.1:c.1829T=	NP_001372182.1:p.Ile610=