Canonical Allele Identifier: CA2817564467

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25892031_25892032insCCCCCCCCCCCCCC , CM000683.2:g.25892031_25892032insCCCCCCCCCCCCCC	GRCh38
NC_000021.8:g.27264343_27264344insCCCCCCCCCCCCCC , CM000683.1:g.27264343_27264344insCCCCCCCCCCCCCC	GRCh37
NC_000021.7:g.26186214_26186215insCCCCCCCCCCCCCC	NCBI36
NG_007376.1:g.283789_283790insGGGGGGGGGGGGGG
NG_007376.2:g.284097_284098insGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2032-164_2032-163insGGGGGGGGGGGGGG
ENST00000707133.1:n.462-164_462-163insGGGGGGGGGGGGGG
ENST00000707134.1:n.731-164_731-163insGGGGGGGGGGGGGG
ENST00000346798.8:c.2065-164_2065-163insGGGGGGGGGGGGGG MANE Select	ENSP00000284981.4:n.2065-164_2065-163insGGGGGGGGGGGGGG
ENST00000346798.7:c.2065-164_2065-163insGGGGGGGGGGGGGG	ENSP00000284981.4:n.2065-164_2065-163insGGGGGGGGGGGGGG
ENST00000348990.9:c.1840-164_1840-163insGGGGGGGGGGGGGG	ENSP00000345463.5:n.1840-164_1840-163insGGGGGGGGGGGGGG
ENST00000354192.7:c.1672-164_1672-163insGGGGGGGGGGGGGG	ENSP00000346129.3:n.1672-164_1672-163insGGGGGGGGGGGGGG
ENST00000357903.7:c.2008-164_2008-163insGGGGGGGGGGGGGG	ENSP00000350578.3:n.2008-164_2008-163insGGGGGGGGGGGGGG
ENST00000358918.7:c.2011-164_2011-163insGGGGGGGGGGGGGG	ENSP00000351796.3:n.2011-164_2011-163insGGGGGGGGGGGGGG
ENST00000359726.7:c.1735-164_1735-163insGGGGGGGGGGGGGG	ENSP00000352760.4:n.1735-164_1735-163insGGGGGGGGGGGGGG
ENST00000439274.6:c.1897-164_1897-163insGGGGGGGGGGGGGG	ENSP00000398879.2:n.1897-164_1897-163insGGGGGGGGGGGGGG
ENST00000440126.7:c.1993-164_1993-163insGGGGGGGGGGGGGG	ENSP00000387483.2:n.1993-164_1993-163insGGGGGGGGGGGGGG
ENST00000464867.1:n.412-164_412-163insGGGGGGGGGGGGGG
NM_000484.3:c.2065-164_2065-163insGGGGGGGGGGGGGG	NP_000475.1:n.2065-164_2065-163insGGGGGGGGGGGGGG
NM_001136016.3:c.1993-164_1993-163insGGGGGGGGGGGGGG	NP_001129488.1:n.1993-164_1993-163insGGGGGGGGGGGGGG
NM_001136129.2:c.1672-164_1672-163insGGGGGGGGGGGGGG	NP_001129601.1:n.1672-164_1672-163insGGGGGGGGGGGGGG
NM_001136130.2:c.1897-164_1897-163insGGGGGGGGGGGGGG	NP_001129602.1:n.1897-164_1897-163insGGGGGGGGGGGGGG
NM_001136131.2:c.1735-164_1735-163insGGGGGGGGGGGGGG	NP_001129603.1:n.1735-164_1735-163insGGGGGGGGGGGGGG
NM_001204301.1:c.2011-164_2011-163insGGGGGGGGGGGGGG	NP_001191230.1:n.2011-164_2011-163insGGGGGGGGGGGGGG
NM_001204302.1:c.1954-164_1954-163insGGGGGGGGGGGGGG	NP_001191231.1:n.1954-164_1954-163insGGGGGGGGGGGGGG
NM_001204303.1:c.1786-164_1786-163insGGGGGGGGGGGGGG	NP_001191232.1:n.1786-164_1786-163insGGGGGGGGGGGGGG
NM_201413.2:c.2008-164_2008-163insGGGGGGGGGGGGGG	NP_958816.1:n.2008-164_2008-163insGGGGGGGGGGGGGG
NM_201414.2:c.1840-164_1840-163insGGGGGGGGGGGGGG	NP_958817.1:n.1840-164_1840-163insGGGGGGGGGGGGGG
NM_000484.4:c.2065-164_2065-163insGGGGGGGGGGGGGG MANE Select	NP_000475.1:n.2065-164_2065-163insGGGGGGGGGGGGGG
NM_001136129.3:c.1672-164_1672-163insGGGGGGGGGGGGGG	NP_001129601.1:n.1672-164_1672-163insGGGGGGGGGGGGGG
NM_001136130.3:c.1897-164_1897-163insGGGGGGGGGGGGGG	NP_001129602.1:n.1897-164_1897-163insGGGGGGGGGGGGGG
NM_001204301.2:c.2011-164_2011-163insGGGGGGGGGGGGGG	NP_001191230.1:n.2011-164_2011-163insGGGGGGGGGGGGGG
NM_001204302.2:c.1954-164_1954-163insGGGGGGGGGGGGGG	NP_001191231.1:n.1954-164_1954-163insGGGGGGGGGGGGGG
NM_001204303.2:c.1786-164_1786-163insGGGGGGGGGGGGGG	NP_001191232.1:n.1786-164_1786-163insGGGGGGGGGGGGGG
NM_201413.3:c.2008-164_2008-163insGGGGGGGGGGGGGG	NP_958816.1:n.2008-164_2008-163insGGGGGGGGGGGGGG
NM_201414.3:c.1840-164_1840-163insGGGGGGGGGGGGGG	NP_958817.1:n.1840-164_1840-163insGGGGGGGGGGGGGG
NM_001136131.3:c.1735-164_1735-163insGGGGGGGGGGGGGG	NP_001129603.1:n.1735-164_1735-163insGGGGGGGGGGGGGG
NM_001385253.1:c.1897-164_1897-163insGGGGGGGGGGGGGG	NP_001372182.1:n.1897-164_1897-163insGGGGGGGGGGGGGG