Canonical Allele Identifier: CA2383554913

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897603G= , CM000683.2:g.25897603G=	GRCh38
NC_000021.8:g.27269915G= , CM000683.1:g.27269915G=	GRCh37
NC_000021.7:g.26191786G=	NCBI36
NG_007376.1:g.278218C=
NG_007376.2:g.278526C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2001C=
ENST00000707133.1:n.431C=
ENST00000707134.1:n.700C=
ENST00000346798.8:c.2034C= MANE Select	ENSP00000284981.4:p.Asp678=
ENST00000346798.7:c.2034C=	ENSP00000284981.4:p.Asp678=
ENST00000348990.9:c.1809C=	ENSP00000345463.5:p.Asp603=
ENST00000354192.7:c.1641C=	ENSP00000346129.3:p.Asp547=
ENST00000357903.7:c.1977C=	ENSP00000350578.3:p.Asp659=
ENST00000358918.7:c.1980C=	ENSP00000351796.3:p.Asp660=
ENST00000359726.7:c.1704C=	ENSP00000352760.4:p.Asp568=
ENST00000439274.6:c.1866C=	ENSP00000398879.2:p.Asp622=
ENST00000440126.7:c.1962C=	ENSP00000387483.2:p.Asp654=
ENST00000464867.1:n.381C=
NM_000484.3:c.2034C=	NP_000475.1:p.Asp678=
NM_001136016.3:c.1962C=	NP_001129488.1:p.Asp654=
NM_001136129.2:c.1641C=	NP_001129601.1:p.Asp547=
NM_001136130.2:c.1866C=	NP_001129602.1:p.Asp622=
NM_001136131.2:c.1704C=	NP_001129603.1:p.Asp568=
NM_001204301.1:c.1980C=	NP_001191230.1:p.Asp660=
NM_001204302.1:c.1923C=	NP_001191231.1:p.Asp641=
NM_001204303.1:c.1755C=	NP_001191232.1:p.Asp585=
NM_201413.2:c.1977C=	NP_958816.1:p.Asp659=
NM_201414.2:c.1809C=	NP_958817.1:p.Asp603=
NM_000484.4:c.2034C= MANE Select	NP_000475.1:p.Asp678=
NM_001136129.3:c.1641C=	NP_001129601.1:p.Asp547=
NM_001136130.3:c.1866C=	NP_001129602.1:p.Asp622=
NM_001204301.2:c.1980C=	NP_001191230.1:p.Asp660=
NM_001204302.2:c.1923C=	NP_001191231.1:p.Asp641=
NM_001204303.2:c.1755C=	NP_001191232.1:p.Asp585=
NM_201413.3:c.1977C=	NP_958816.1:p.Asp659=
NM_201414.3:c.1809C=	NP_958817.1:p.Asp603=
NM_001136131.3:c.1704C=	NP_001129603.1:p.Asp568=
NM_001385253.1:c.1866C=	NP_001372182.1:p.Asp622=