Canonical Allele Identifier: CA2654122769

Gene: APP

Linked Data

• gnomAD v4: 21-25891978-TGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891980_25891982del , CM000683.2:g.25891980_25891982del	GRCh38
NC_000021.8:g.27264292_27264294del , CM000683.1:g.27264292_27264294del	GRCh37
NC_000021.7:g.26186163_26186165del	NCBI36
NG_007376.1:g.283840_283842del
NG_007376.2:g.284148_284150del

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2032-113_2032-111del
ENST00000707133.1:n.462-113_462-111del
ENST00000707134.1:n.731-113_731-111del
ENST00000346798.8:c.2065-113_2065-111del MANE Select	ENSP00000284981.4:n.2065-113_2065-111del
ENST00000346798.7:c.2065-113_2065-111del	ENSP00000284981.4:n.2065-113_2065-111del
ENST00000348990.9:c.1840-113_1840-111del	ENSP00000345463.5:n.1840-113_1840-111del
ENST00000354192.7:c.1672-113_1672-111del	ENSP00000346129.3:n.1672-113_1672-111del
ENST00000357903.7:c.2008-113_2008-111del	ENSP00000350578.3:n.2008-113_2008-111del
ENST00000358918.7:c.2011-113_2011-111del	ENSP00000351796.3:n.2011-113_2011-111del
ENST00000359726.7:c.1735-113_1735-111del	ENSP00000352760.4:n.1735-113_1735-111del
ENST00000439274.6:c.1897-113_1897-111del	ENSP00000398879.2:n.1897-113_1897-111del
ENST00000440126.7:c.1993-113_1993-111del	ENSP00000387483.2:n.1993-113_1993-111del
ENST00000464867.1:n.412-113_412-111del
NM_000484.3:c.2065-113_2065-111del	NP_000475.1:n.2065-113_2065-111del
NM_001136016.3:c.1993-113_1993-111del	NP_001129488.1:n.1993-113_1993-111del
NM_001136129.2:c.1672-113_1672-111del	NP_001129601.1:n.1672-113_1672-111del
NM_001136130.2:c.1897-113_1897-111del	NP_001129602.1:n.1897-113_1897-111del
NM_001136131.2:c.1735-113_1735-111del	NP_001129603.1:n.1735-113_1735-111del
NM_001204301.1:c.2011-113_2011-111del	NP_001191230.1:n.2011-113_2011-111del
NM_001204302.1:c.1954-113_1954-111del	NP_001191231.1:n.1954-113_1954-111del
NM_001204303.1:c.1786-113_1786-111del	NP_001191232.1:n.1786-113_1786-111del
NM_201413.2:c.2008-113_2008-111del	NP_958816.1:n.2008-113_2008-111del
NM_201414.2:c.1840-113_1840-111del	NP_958817.1:n.1840-113_1840-111del
NM_000484.4:c.2065-113_2065-111del MANE Select	NP_000475.1:n.2065-113_2065-111del
NM_001136129.3:c.1672-113_1672-111del	NP_001129601.1:n.1672-113_1672-111del
NM_001136130.3:c.1897-113_1897-111del	NP_001129602.1:n.1897-113_1897-111del
NM_001204301.2:c.2011-113_2011-111del	NP_001191230.1:n.2011-113_2011-111del
NM_001204302.2:c.1954-113_1954-111del	NP_001191231.1:n.1954-113_1954-111del
NM_001204303.2:c.1786-113_1786-111del	NP_001191232.1:n.1786-113_1786-111del
NM_201413.3:c.2008-113_2008-111del	NP_958816.1:n.2008-113_2008-111del
NM_201414.3:c.1840-113_1840-111del	NP_958817.1:n.1840-113_1840-111del
NM_001136131.3:c.1735-113_1735-111del	NP_001129603.1:n.1735-113_1735-111del
NM_001385253.1:c.1897-113_1897-111del	NP_001372182.1:n.1897-113_1897-111del