Canonical Allele Identifier: CA2383551942

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25892397_25892399delinsCTT , CM000683.2:g.25892397_25892399delinsCTT	GRCh38
NC_000021.8:g.27264709_27264711delinsCTT , CM000683.1:g.27264709_27264711delinsCTT	GRCh37
NC_000021.7:g.26186580_26186582delinsCTT	NCBI36
NG_007376.1:g.283422_283424delinsAAG
NG_007376.2:g.283730_283732delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2032-531_2032-529delinsAAG
ENST00000707133.1:n.462-531_462-529delinsAAG
ENST00000707134.1:n.731-531_731-529delinsAAG
ENST00000346798.8:c.2065-531_2065-529delinsAAG MANE Select	ENSP00000284981.4:n.2065-531_2065-529delinsAAG
ENST00000346798.7:c.2065-531_2065-529delinsAAG	ENSP00000284981.4:n.2065-531_2065-529delinsAAG
ENST00000348990.9:c.1840-531_1840-529delinsAAG	ENSP00000345463.5:n.1840-531_1840-529delinsAAG
ENST00000354192.7:c.1672-531_1672-529delinsAAG	ENSP00000346129.3:n.1672-531_1672-529delinsAAG
ENST00000357903.7:c.2008-531_2008-529delinsAAG	ENSP00000350578.3:n.2008-531_2008-529delinsAAG
ENST00000358918.7:c.2011-531_2011-529delinsAAG	ENSP00000351796.3:n.2011-531_2011-529delinsAAG
ENST00000359726.7:c.1735-531_1735-529delinsAAG	ENSP00000352760.4:n.1735-531_1735-529delinsAAG
ENST00000439274.6:c.1897-531_1897-529delinsAAG	ENSP00000398879.2:n.1897-531_1897-529delinsAAG
ENST00000440126.7:c.1993-531_1993-529delinsAAG	ENSP00000387483.2:n.1993-531_1993-529delinsAAG
ENST00000464867.1:n.412-531_412-529delinsAAG
NM_000484.3:c.2065-531_2065-529delinsAAG	NP_000475.1:n.2065-531_2065-529delinsAAG
NM_001136016.3:c.1993-531_1993-529delinsAAG	NP_001129488.1:n.1993-531_1993-529delinsAAG
NM_001136129.2:c.1672-531_1672-529delinsAAG	NP_001129601.1:n.1672-531_1672-529delinsAAG
NM_001136130.2:c.1897-531_1897-529delinsAAG	NP_001129602.1:n.1897-531_1897-529delinsAAG
NM_001136131.2:c.1735-531_1735-529delinsAAG	NP_001129603.1:n.1735-531_1735-529delinsAAG
NM_001204301.1:c.2011-531_2011-529delinsAAG	NP_001191230.1:n.2011-531_2011-529delinsAAG
NM_001204302.1:c.1954-531_1954-529delinsAAG	NP_001191231.1:n.1954-531_1954-529delinsAAG
NM_001204303.1:c.1786-531_1786-529delinsAAG	NP_001191232.1:n.1786-531_1786-529delinsAAG
NM_201413.2:c.2008-531_2008-529delinsAAG	NP_958816.1:n.2008-531_2008-529delinsAAG
NM_201414.2:c.1840-531_1840-529delinsAAG	NP_958817.1:n.1840-531_1840-529delinsAAG
NM_000484.4:c.2065-531_2065-529delinsAAG MANE Select	NP_000475.1:n.2065-531_2065-529delinsAAG
NM_001136129.3:c.1672-531_1672-529delinsAAG	NP_001129601.1:n.1672-531_1672-529delinsAAG
NM_001136130.3:c.1897-531_1897-529delinsAAG	NP_001129602.1:n.1897-531_1897-529delinsAAG
NM_001204301.2:c.2011-531_2011-529delinsAAG	NP_001191230.1:n.2011-531_2011-529delinsAAG
NM_001204302.2:c.1954-531_1954-529delinsAAG	NP_001191231.1:n.1954-531_1954-529delinsAAG
NM_001204303.2:c.1786-531_1786-529delinsAAG	NP_001191232.1:n.1786-531_1786-529delinsAAG
NM_201413.3:c.2008-531_2008-529delinsAAG	NP_958816.1:n.2008-531_2008-529delinsAAG
NM_201414.3:c.1840-531_1840-529delinsAAG	NP_958817.1:n.1840-531_1840-529delinsAAG
NM_001136131.3:c.1735-531_1735-529delinsAAG	NP_001129603.1:n.1735-531_1735-529delinsAAG
NM_001385253.1:c.1897-531_1897-529delinsAAG	NP_001372182.1:n.1897-531_1897-529delinsAAG