Canonical Allele Identifier: CA2383554948

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897655A= , CM000683.2:g.25897655A=	GRCh38
NC_000021.8:g.27269967A= , CM000683.1:g.27269967A=	GRCh37
NC_000021.7:g.26191838A=	NCBI36
NG_007376.1:g.278166T=
NG_007376.2:g.278474T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.1949T=
ENST00000707133.1:n.379T=
ENST00000707134.1:n.648T=
ENST00000346798.8:c.1982T= MANE Select	ENSP00000284981.4:p.Ile661=
ENST00000346798.7:c.1982T=	ENSP00000284981.4:p.Ile661=
ENST00000348990.9:c.1757T=	ENSP00000345463.5:p.Ile586=
ENST00000354192.7:c.1589T=	ENSP00000346129.3:p.Ile530=
ENST00000357903.7:c.1925T=	ENSP00000350578.3:p.Ile642=
ENST00000358918.7:c.1928T=	ENSP00000351796.3:p.Ile643=
ENST00000359726.7:c.1652T=	ENSP00000352760.4:p.Ile551=
ENST00000439274.6:c.1814T=	ENSP00000398879.2:p.Ile605=
ENST00000440126.7:c.1910T=	ENSP00000387483.2:p.Ile637=
ENST00000464867.1:n.329T=
NM_000484.3:c.1982T=	NP_000475.1:p.Ile661=
NM_001136016.3:c.1910T=	NP_001129488.1:p.Ile637=
NM_001136129.2:c.1589T=	NP_001129601.1:p.Ile530=
NM_001136130.2:c.1814T=	NP_001129602.1:p.Ile605=
NM_001136131.2:c.1652T=	NP_001129603.1:p.Ile551=
NM_001204301.1:c.1928T=	NP_001191230.1:p.Ile643=
NM_001204302.1:c.1871T=	NP_001191231.1:p.Ile624=
NM_001204303.1:c.1703T=	NP_001191232.1:p.Ile568=
NM_201413.2:c.1925T=	NP_958816.1:p.Ile642=
NM_201414.2:c.1757T=	NP_958817.1:p.Ile586=
NM_000484.4:c.1982T= MANE Select	NP_000475.1:p.Ile661=
NM_001136129.3:c.1589T=	NP_001129601.1:p.Ile530=
NM_001136130.3:c.1814T=	NP_001129602.1:p.Ile605=
NM_001204301.2:c.1928T=	NP_001191230.1:p.Ile643=
NM_001204302.2:c.1871T=	NP_001191231.1:p.Ile624=
NM_001204303.2:c.1703T=	NP_001191232.1:p.Ile568=
NM_201413.3:c.1925T=	NP_958816.1:p.Ile642=
NM_201414.3:c.1757T=	NP_958817.1:p.Ile586=
NM_001136131.3:c.1652T=	NP_001129603.1:p.Ile551=
NM_001385253.1:c.1814T=	NP_001372182.1:p.Ile605=