Canonical Allele Identifier: CA637162704

Gene: APP

Linked Data

• dbSNP Id: rs1208893762
• gnomAD v2: 21-27264371-AAAAAAAG-A
• gnomAD v3: 21-25892059-AAAAAAAG-A
• gnomAD v4: 21-25892059-AAAAAAAG-A
• MyVariant Identifiers: chr21:g.27264372_27264378del (hg19) ; chr21:g.25892060_25892066del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25892063_25892069del , CM000683.2:g.25892063_25892069del	GRCh38
NC_000021.8:g.27264375_27264381del , CM000683.1:g.27264375_27264381del	GRCh37
NC_000021.7:g.26186246_26186252del	NCBI36
NG_007376.1:g.283755_283761del
NG_007376.2:g.284063_284069del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2032-198_2032-192del
ENST00000707133.1:n.462-198_462-192del
ENST00000707134.1:n.731-198_731-192del
ENST00000346798.8:c.2065-198_2065-192del MANE Select	ENSP00000284981.4:n.2065-198_2065-192del
ENST00000346798.7:c.2065-198_2065-192del	ENSP00000284981.4:n.2065-198_2065-192del
ENST00000348990.9:c.1840-198_1840-192del	ENSP00000345463.5:n.1840-198_1840-192del
ENST00000354192.7:c.1672-198_1672-192del	ENSP00000346129.3:n.1672-198_1672-192del
ENST00000357903.7:c.2008-198_2008-192del	ENSP00000350578.3:n.2008-198_2008-192del
ENST00000358918.7:c.2011-198_2011-192del	ENSP00000351796.3:n.2011-198_2011-192del
ENST00000359726.7:c.1735-198_1735-192del	ENSP00000352760.4:n.1735-198_1735-192del
ENST00000439274.6:c.1897-198_1897-192del	ENSP00000398879.2:n.1897-198_1897-192del
ENST00000440126.7:c.1993-198_1993-192del	ENSP00000387483.2:n.1993-198_1993-192del
ENST00000464867.1:n.412-198_412-192del
NM_000484.3:c.2065-198_2065-192del	NP_000475.1:n.2065-198_2065-192del
NM_001136016.3:c.1993-198_1993-192del	NP_001129488.1:n.1993-198_1993-192del
NM_001136129.2:c.1672-198_1672-192del	NP_001129601.1:n.1672-198_1672-192del
NM_001136130.2:c.1897-198_1897-192del	NP_001129602.1:n.1897-198_1897-192del
NM_001136131.2:c.1735-198_1735-192del	NP_001129603.1:n.1735-198_1735-192del
NM_001204301.1:c.2011-198_2011-192del	NP_001191230.1:n.2011-198_2011-192del
NM_001204302.1:c.1954-198_1954-192del	NP_001191231.1:n.1954-198_1954-192del
NM_001204303.1:c.1786-198_1786-192del	NP_001191232.1:n.1786-198_1786-192del
NM_201413.2:c.2008-198_2008-192del	NP_958816.1:n.2008-198_2008-192del
NM_201414.2:c.1840-198_1840-192del	NP_958817.1:n.1840-198_1840-192del
NM_000484.4:c.2065-198_2065-192del MANE Select	NP_000475.1:n.2065-198_2065-192del
NM_001136129.3:c.1672-198_1672-192del	NP_001129601.1:n.1672-198_1672-192del
NM_001136130.3:c.1897-198_1897-192del	NP_001129602.1:n.1897-198_1897-192del
NM_001204301.2:c.2011-198_2011-192del	NP_001191230.1:n.2011-198_2011-192del
NM_001204302.2:c.1954-198_1954-192del	NP_001191231.1:n.1954-198_1954-192del
NM_001204303.2:c.1786-198_1786-192del	NP_001191232.1:n.1786-198_1786-192del
NM_201413.3:c.2008-198_2008-192del	NP_958816.1:n.2008-198_2008-192del
NM_201414.3:c.1840-198_1840-192del	NP_958817.1:n.1840-198_1840-192del
NM_001136131.3:c.1735-198_1735-192del	NP_001129603.1:n.1735-198_1735-192del
NM_001385253.1:c.1897-198_1897-192del	NP_001372182.1:n.1897-198_1897-192del