Canonical Allele Identifier: CA2383551635

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891829T= , CM000683.2:g.25891829T=	GRCh38
NC_000021.8:g.27264141T= , CM000683.1:g.27264141T=	GRCh37
NC_000021.7:g.26186012T=	NCBI36
NG_007376.1:g.283992A=
NG_007376.2:g.284300A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2071A=
ENST00000707133.1:n.501A=
ENST00000707134.1:n.770A=
ENST00000346798.8:c.2104A= MANE Select	ENSP00000284981.4:p.Ile702=
ENST00000346798.7:c.2104A=	ENSP00000284981.4:p.Ile702=
ENST00000348990.9:c.1879A=	ENSP00000345463.5:p.Ile627=
ENST00000354192.7:c.1711A=	ENSP00000346129.3:p.Ile571=
ENST00000357903.7:c.2047A=	ENSP00000350578.3:p.Ile683=
ENST00000358918.7:c.2050A=	ENSP00000351796.3:p.Ile684=
ENST00000359726.7:c.1774A=	ENSP00000352760.4:p.Ile592=
ENST00000439274.6:c.1936A=	ENSP00000398879.2:p.Ile646=
ENST00000440126.7:c.2032A=	ENSP00000387483.2:p.Ile678=
ENST00000464867.1:n.451A=
NM_000484.3:c.2104A=	NP_000475.1:p.Ile702=
NM_001136016.3:c.2032A=	NP_001129488.1:p.Ile678=
NM_001136129.2:c.1711A=	NP_001129601.1:p.Ile571=
NM_001136130.2:c.1936A=	NP_001129602.1:p.Ile646=
NM_001136131.2:c.1774A=	NP_001129603.1:p.Ile592=
NM_001204301.1:c.2050A=	NP_001191230.1:p.Ile684=
NM_001204302.1:c.1993A=	NP_001191231.1:p.Ile665=
NM_001204303.1:c.1825A=	NP_001191232.1:p.Ile609=
NM_201413.2:c.2047A=	NP_958816.1:p.Ile683=
NM_201414.2:c.1879A=	NP_958817.1:p.Ile627=
NM_000484.4:c.2104A= MANE Select	NP_000475.1:p.Ile702=
NM_001136129.3:c.1711A=	NP_001129601.1:p.Ile571=
NM_001136130.3:c.1936A=	NP_001129602.1:p.Ile646=
NM_001204301.2:c.2050A=	NP_001191230.1:p.Ile684=
NM_001204302.2:c.1993A=	NP_001191231.1:p.Ile665=
NM_001204303.2:c.1825A=	NP_001191232.1:p.Ile609=
NM_201413.3:c.2047A=	NP_958816.1:p.Ile683=
NM_201414.3:c.1879A=	NP_958817.1:p.Ile627=
NM_001136131.3:c.1774A=	NP_001129603.1:p.Ile592=
NM_001385253.1:c.1936A=	NP_001372182.1:p.Ile646=