Canonical Allele Identifier: CA2383554950

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897657A= , CM000683.2:g.25897657A=	GRCh38
NC_000021.8:g.27269969A= , CM000683.1:g.27269969A=	GRCh37
NC_000021.7:g.26191840A=	NCBI36
NG_007376.1:g.278164T=
NG_007376.2:g.278472T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.1947T=
ENST00000707133.1:n.377T=
ENST00000707134.1:n.646T=
ENST00000346798.8:c.1980T= MANE Select	ENSP00000284981.4:p.Asn660=
ENST00000346798.7:c.1980T=	ENSP00000284981.4:p.Asn660=
ENST00000348990.9:c.1755T=	ENSP00000345463.5:p.Asn585=
ENST00000354192.7:c.1587T=	ENSP00000346129.3:p.Asn529=
ENST00000357903.7:c.1923T=	ENSP00000350578.3:p.Asn641=
ENST00000358918.7:c.1926T=	ENSP00000351796.3:p.Asn642=
ENST00000359726.7:c.1650T=	ENSP00000352760.4:p.Asn550=
ENST00000439274.6:c.1812T=	ENSP00000398879.2:p.Asn604=
ENST00000440126.7:c.1908T=	ENSP00000387483.2:p.Asn636=
ENST00000464867.1:n.327T=
NM_000484.3:c.1980T=	NP_000475.1:p.Asn660=
NM_001136016.3:c.1908T=	NP_001129488.1:p.Asn636=
NM_001136129.2:c.1587T=	NP_001129601.1:p.Asn529=
NM_001136130.2:c.1812T=	NP_001129602.1:p.Asn604=
NM_001136131.2:c.1650T=	NP_001129603.1:p.Asn550=
NM_001204301.1:c.1926T=	NP_001191230.1:p.Asn642=
NM_001204302.1:c.1869T=	NP_001191231.1:p.Asn623=
NM_001204303.1:c.1701T=	NP_001191232.1:p.Asn567=
NM_201413.2:c.1923T=	NP_958816.1:p.Asn641=
NM_201414.2:c.1755T=	NP_958817.1:p.Asn585=
NM_000484.4:c.1980T= MANE Select	NP_000475.1:p.Asn660=
NM_001136129.3:c.1587T=	NP_001129601.1:p.Asn529=
NM_001136130.3:c.1812T=	NP_001129602.1:p.Asn604=
NM_001204301.2:c.1926T=	NP_001191230.1:p.Asn642=
NM_001204302.2:c.1869T=	NP_001191231.1:p.Asn623=
NM_001204303.2:c.1701T=	NP_001191232.1:p.Asn567=
NM_201413.3:c.1923T=	NP_958816.1:p.Asn641=
NM_201414.3:c.1755T=	NP_958817.1:p.Asn585=
NM_001136131.3:c.1650T=	NP_001129603.1:p.Asn550=
NM_001385253.1:c.1812T=	NP_001372182.1:p.Asn604=