Canonical Allele Identifier: CA2817564551

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25892359_25892361del , CM000683.2:g.25892359_25892361del	GRCh38
NC_000021.8:g.27264671_27264673del , CM000683.1:g.27264671_27264673del	GRCh37
NC_000021.7:g.26186542_26186544del	NCBI36
NG_007376.1:g.283460_283462del
NG_007376.2:g.283768_283770del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2032-493_2032-491del
ENST00000707133.1:n.462-493_462-491del
ENST00000707134.1:n.731-493_731-491del
ENST00000346798.8:c.2065-493_2065-491del MANE Select	ENSP00000284981.4:n.2065-493_2065-491del
ENST00000346798.7:c.2065-493_2065-491del	ENSP00000284981.4:n.2065-493_2065-491del
ENST00000348990.9:c.1840-493_1840-491del	ENSP00000345463.5:n.1840-493_1840-491del
ENST00000354192.7:c.1672-493_1672-491del	ENSP00000346129.3:n.1672-493_1672-491del
ENST00000357903.7:c.2008-493_2008-491del	ENSP00000350578.3:n.2008-493_2008-491del
ENST00000358918.7:c.2011-493_2011-491del	ENSP00000351796.3:n.2011-493_2011-491del
ENST00000359726.7:c.1735-493_1735-491del	ENSP00000352760.4:n.1735-493_1735-491del
ENST00000439274.6:c.1897-493_1897-491del	ENSP00000398879.2:n.1897-493_1897-491del
ENST00000440126.7:c.1993-493_1993-491del	ENSP00000387483.2:n.1993-493_1993-491del
ENST00000464867.1:n.412-493_412-491del
NM_000484.3:c.2065-493_2065-491del	NP_000475.1:n.2065-493_2065-491del
NM_001136016.3:c.1993-493_1993-491del	NP_001129488.1:n.1993-493_1993-491del
NM_001136129.2:c.1672-493_1672-491del	NP_001129601.1:n.1672-493_1672-491del
NM_001136130.2:c.1897-493_1897-491del	NP_001129602.1:n.1897-493_1897-491del
NM_001136131.2:c.1735-493_1735-491del	NP_001129603.1:n.1735-493_1735-491del
NM_001204301.1:c.2011-493_2011-491del	NP_001191230.1:n.2011-493_2011-491del
NM_001204302.1:c.1954-493_1954-491del	NP_001191231.1:n.1954-493_1954-491del
NM_001204303.1:c.1786-493_1786-491del	NP_001191232.1:n.1786-493_1786-491del
NM_201413.2:c.2008-493_2008-491del	NP_958816.1:n.2008-493_2008-491del
NM_201414.2:c.1840-493_1840-491del	NP_958817.1:n.1840-493_1840-491del
NM_000484.4:c.2065-493_2065-491del MANE Select	NP_000475.1:n.2065-493_2065-491del
NM_001136129.3:c.1672-493_1672-491del	NP_001129601.1:n.1672-493_1672-491del
NM_001136130.3:c.1897-493_1897-491del	NP_001129602.1:n.1897-493_1897-491del
NM_001204301.2:c.2011-493_2011-491del	NP_001191230.1:n.2011-493_2011-491del
NM_001204302.2:c.1954-493_1954-491del	NP_001191231.1:n.1954-493_1954-491del
NM_001204303.2:c.1786-493_1786-491del	NP_001191232.1:n.1786-493_1786-491del
NM_201413.3:c.2008-493_2008-491del	NP_958816.1:n.2008-493_2008-491del
NM_201414.3:c.1840-493_1840-491del	NP_958817.1:n.1840-493_1840-491del
NM_001136131.3:c.1735-493_1735-491del	NP_001129603.1:n.1735-493_1735-491del
NM_001385253.1:c.1897-493_1897-491del	NP_001372182.1:n.1897-493_1897-491del