Canonical Allele Identifier: CA3243796650

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891791T= , CM000683.2:g.25891791T=	GRCh38
NC_000021.8:g.27264103T= , CM000683.1:g.27264103T=	GRCh37
NC_000021.7:g.26185974T=	NCBI36
NG_007376.1:g.284030A=
NG_007376.2:g.284338A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000484.4:c.2142A= MANE Select	NP_000475.1:p.Thr714=
ENST00000346798.8:c.2142A= MANE Select	ENSP00000284981.4:p.Thr714=
NM_000484.3:c.2142A=	NP_000475.1:p.Thr714=
NM_001136016.3:c.2070A=	NP_001129488.1:p.Thr690=
NM_001136129.2:c.1749A=	NP_001129601.1:p.Thr583=
NM_001136129.3:c.1749A=	NP_001129601.1:p.Thr583=
NM_001136130.2:c.1974A=	NP_001129602.1:p.Thr658=
NM_001136130.3:c.1974A=	NP_001129602.1:p.Thr658=
NM_001136131.2:c.1812A=	NP_001129603.1:p.Thr604=
NM_001136131.3:c.1812A=	NP_001129603.1:p.Thr604=
NM_001204301.1:c.2088A=	NP_001191230.1:p.Thr696=
NM_001204301.2:c.2088A=	NP_001191230.1:p.Thr696=
NM_001204302.1:c.2031A=	NP_001191231.1:p.Thr677=
NM_001204302.2:c.2031A=	NP_001191231.1:p.Thr677=
NM_001204303.1:c.1863A=	NP_001191232.1:p.Thr621=
NM_001204303.2:c.1863A=	NP_001191232.1:p.Thr621=
NM_001385253.1:c.1974A=	NP_001372182.1:p.Thr658=
NM_201413.2:c.2085A=	NP_958816.1:p.Thr695=
NM_201413.3:c.2085A=	NP_958816.1:p.Thr695=
NM_201414.2:c.1917A=	NP_958817.1:p.Thr639=
NM_201414.3:c.1917A=	NP_958817.1:p.Thr639=
ENST00000346798.7:c.2142A=	ENSP00000284981.4:p.Thr714=
ENST00000348990.9:c.1917A=	ENSP00000345463.5:p.Thr639=
ENST00000354192.7:c.1749A=	ENSP00000346129.3:p.Thr583=
ENST00000357903.7:c.2085A=	ENSP00000350578.3:p.Thr695=
ENST00000358918.7:c.2088A=	ENSP00000351796.3:p.Thr696=
ENST00000359726.7:c.1812A=	ENSP00000352760.4:p.Thr604=
ENST00000439274.6:c.1974A=	ENSP00000398879.2:p.Thr658=
ENST00000440126.7:c.2070A=	ENSP00000387483.2:p.Thr690=
ENST00000464867.1:n.489A=
ENST00000707132.1:n.2109A=
ENST00000707133.1:n.539A=
ENST00000707134.1:n.808A=