Canonical Allele Identifier: CA2830561775

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891782_25891783insCTG , CM000683.2:g.25891782_25891783insCTG	GRCh38
NC_000021.8:g.27264094_27264095insCTG , CM000683.1:g.27264094_27264095insCTG	GRCh37
NC_000021.7:g.26185965_26185966insCTG	NCBI36
NG_007376.1:g.284040_284041insGCA
NG_007376.2:g.284348_284349insGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2119_2120insGCA
ENST00000707133.1:n.549_550insGCA
ENST00000707134.1:n.818_819insGCA
ENST00000346798.8:c.2152_2153insGCA MANE Select	ENSP00000284981.4:p.Val717_Ile718insSer
ENST00000346798.7:c.2152_2153insGCA	ENSP00000284981.4:p.Val717_Ile718insSer
ENST00000348990.9:c.1927_1928insGCA	ENSP00000345463.5:p.Val642_Ile643insSer
ENST00000354192.7:c.1759_1760insGCA	ENSP00000346129.3:p.Val586_Ile587insSer
ENST00000357903.7:c.2095_2096insGCA	ENSP00000350578.3:p.Val698_Ile699insSer
ENST00000358918.7:c.2098_2099insGCA	ENSP00000351796.3:p.Val699_Ile700insSer
ENST00000359726.7:c.1822_1823insGCA	ENSP00000352760.4:p.Val607_Ile608insSer
ENST00000439274.6:c.1984_1985insGCA	ENSP00000398879.2:p.Val661_Ile662insSer
ENST00000440126.7:c.2080_2081insGCA	ENSP00000387483.2:p.Val693_Ile694insSer
ENST00000464867.1:n.499_500insGCA
NM_000484.3:c.2152_2153insGCA	NP_000475.1:p.Val717_Ile718insSer
NM_001136016.3:c.2080_2081insGCA	NP_001129488.1:p.Val693_Ile694insSer
NM_001136129.2:c.1759_1760insGCA	NP_001129601.1:p.Val586_Ile587insSer
NM_001136130.2:c.1984_1985insGCA	NP_001129602.1:p.Val661_Ile662insSer
NM_001136131.2:c.1822_1823insGCA	NP_001129603.1:p.Val607_Ile608insSer
NM_001204301.1:c.2098_2099insGCA	NP_001191230.1:p.Val699_Ile700insSer
NM_001204302.1:c.2041_2042insGCA	NP_001191231.1:p.Val680_Ile681insSer
NM_001204303.1:c.1873_1874insGCA	NP_001191232.1:p.Val624_Ile625insSer
NM_201413.2:c.2095_2096insGCA	NP_958816.1:p.Val698_Ile699insSer
NM_201414.2:c.1927_1928insGCA	NP_958817.1:p.Val642_Ile643insSer
NM_000484.4:c.2152_2153insGCA MANE Select	NP_000475.1:p.Val717_Ile718insSer
NM_001136129.3:c.1759_1760insGCA	NP_001129601.1:p.Val586_Ile587insSer
NM_001136130.3:c.1984_1985insGCA	NP_001129602.1:p.Val661_Ile662insSer
NM_001204301.2:c.2098_2099insGCA	NP_001191230.1:p.Val699_Ile700insSer
NM_001204302.2:c.2041_2042insGCA	NP_001191231.1:p.Val680_Ile681insSer
NM_001204303.2:c.1873_1874insGCA	NP_001191232.1:p.Val624_Ile625insSer
NM_201413.3:c.2095_2096insGCA	NP_958816.1:p.Val698_Ile699insSer
NM_201414.3:c.1927_1928insGCA	NP_958817.1:p.Val642_Ile643insSer
NM_001136131.3:c.1822_1823insGCA	NP_001129603.1:p.Val607_Ile608insSer
NM_001385253.1:c.1984_1985insGCA	NP_001372182.1:p.Val661_Ile662insSer