Canonical Allele Identifier: CA2817564462

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25892019_25892032del , CM000683.2:g.25892019_25892032del	GRCh38
NC_000021.8:g.27264331_27264344del , CM000683.1:g.27264331_27264344del	GRCh37
NC_000021.7:g.26186202_26186215del	NCBI36
NG_007376.1:g.283790_283803del
NG_007376.2:g.284098_284111del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2032-163_2032-150del
ENST00000707133.1:n.462-163_462-150del
ENST00000707134.1:n.731-163_731-150del
ENST00000346798.8:c.2065-163_2065-150del MANE Select	ENSP00000284981.4:n.2065-163_2065-150del
ENST00000346798.7:c.2065-163_2065-150del	ENSP00000284981.4:n.2065-163_2065-150del
ENST00000348990.9:c.1840-163_1840-150del	ENSP00000345463.5:n.1840-163_1840-150del
ENST00000354192.7:c.1672-163_1672-150del	ENSP00000346129.3:n.1672-163_1672-150del
ENST00000357903.7:c.2008-163_2008-150del	ENSP00000350578.3:n.2008-163_2008-150del
ENST00000358918.7:c.2011-163_2011-150del	ENSP00000351796.3:n.2011-163_2011-150del
ENST00000359726.7:c.1735-163_1735-150del	ENSP00000352760.4:n.1735-163_1735-150del
ENST00000439274.6:c.1897-163_1897-150del	ENSP00000398879.2:n.1897-163_1897-150del
ENST00000440126.7:c.1993-163_1993-150del	ENSP00000387483.2:n.1993-163_1993-150del
ENST00000464867.1:n.412-163_412-150del
NM_000484.3:c.2065-163_2065-150del	NP_000475.1:n.2065-163_2065-150del
NM_001136016.3:c.1993-163_1993-150del	NP_001129488.1:n.1993-163_1993-150del
NM_001136129.2:c.1672-163_1672-150del	NP_001129601.1:n.1672-163_1672-150del
NM_001136130.2:c.1897-163_1897-150del	NP_001129602.1:n.1897-163_1897-150del
NM_001136131.2:c.1735-163_1735-150del	NP_001129603.1:n.1735-163_1735-150del
NM_001204301.1:c.2011-163_2011-150del	NP_001191230.1:n.2011-163_2011-150del
NM_001204302.1:c.1954-163_1954-150del	NP_001191231.1:n.1954-163_1954-150del
NM_001204303.1:c.1786-163_1786-150del	NP_001191232.1:n.1786-163_1786-150del
NM_201413.2:c.2008-163_2008-150del	NP_958816.1:n.2008-163_2008-150del
NM_201414.2:c.1840-163_1840-150del	NP_958817.1:n.1840-163_1840-150del
NM_000484.4:c.2065-163_2065-150del MANE Select	NP_000475.1:n.2065-163_2065-150del
NM_001136129.3:c.1672-163_1672-150del	NP_001129601.1:n.1672-163_1672-150del
NM_001136130.3:c.1897-163_1897-150del	NP_001129602.1:n.1897-163_1897-150del
NM_001204301.2:c.2011-163_2011-150del	NP_001191230.1:n.2011-163_2011-150del
NM_001204302.2:c.1954-163_1954-150del	NP_001191231.1:n.1954-163_1954-150del
NM_001204303.2:c.1786-163_1786-150del	NP_001191232.1:n.1786-163_1786-150del
NM_201413.3:c.2008-163_2008-150del	NP_958816.1:n.2008-163_2008-150del
NM_201414.3:c.1840-163_1840-150del	NP_958817.1:n.1840-163_1840-150del
NM_001136131.3:c.1735-163_1735-150del	NP_001129603.1:n.1735-163_1735-150del
NM_001385253.1:c.1897-163_1897-150del	NP_001372182.1:n.1897-163_1897-150del