Canonical Allele Identifier: CA2383554934

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897632C= , CM000683.2:g.25897632C=	GRCh38
NC_000021.8:g.27269944C= , CM000683.1:g.27269944C=	GRCh37
NC_000021.7:g.26191815C=	NCBI36
NG_007376.1:g.278189G=
NG_007376.2:g.278497G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1972G=
ENST00000707133.1:n.402G=
ENST00000707134.1:n.671G=
ENST00000346798.8:c.2005G= MANE Select	ENSP00000284981.4:p.Val669=
ENST00000346798.7:c.2005G=	ENSP00000284981.4:p.Val669=
ENST00000348990.9:c.1780G=	ENSP00000345463.5:p.Val594=
ENST00000354192.7:c.1612G=	ENSP00000346129.3:p.Val538=
ENST00000357903.7:c.1948G=	ENSP00000350578.3:p.Val650=
ENST00000358918.7:c.1951G=	ENSP00000351796.3:p.Val651=
ENST00000359726.7:c.1675G=	ENSP00000352760.4:p.Val559=
ENST00000439274.6:c.1837G=	ENSP00000398879.2:p.Val613=
ENST00000440126.7:c.1933G=	ENSP00000387483.2:p.Val645=
ENST00000464867.1:n.352G=
NM_000484.3:c.2005G=	NP_000475.1:p.Val669=
NM_001136016.3:c.1933G=	NP_001129488.1:p.Val645=
NM_001136129.2:c.1612G=	NP_001129601.1:p.Val538=
NM_001136130.2:c.1837G=	NP_001129602.1:p.Val613=
NM_001136131.2:c.1675G=	NP_001129603.1:p.Val559=
NM_001204301.1:c.1951G=	NP_001191230.1:p.Val651=
NM_001204302.1:c.1894G=	NP_001191231.1:p.Val632=
NM_001204303.1:c.1726G=	NP_001191232.1:p.Val576=
NM_201413.2:c.1948G=	NP_958816.1:p.Val650=
NM_201414.2:c.1780G=	NP_958817.1:p.Val594=
NM_000484.4:c.2005G= MANE Select	NP_000475.1:p.Val669=
NM_001136129.3:c.1612G=	NP_001129601.1:p.Val538=
NM_001136130.3:c.1837G=	NP_001129602.1:p.Val613=
NM_001204301.2:c.1951G=	NP_001191230.1:p.Val651=
NM_001204302.2:c.1894G=	NP_001191231.1:p.Val632=
NM_001204303.2:c.1726G=	NP_001191232.1:p.Val576=
NM_201413.3:c.1948G=	NP_958816.1:p.Val650=
NM_201414.3:c.1780G=	NP_958817.1:p.Val594=
NM_001136131.3:c.1675G=	NP_001129603.1:p.Val559=
NM_001385253.1:c.1837G=	NP_001372182.1:p.Val613=