Canonical Allele Identifier: CA9987066

Gene: APP

Linked Data

• dbSNP Id: rs747973071
• ExAC: 21:27264193 TTAAGAA / T
• gnomAD v2: 21-27264193-TTAAGAA-T
• gnomAD v3: 21-25891881-TTAAGAA-T
• gnomAD v4: 21-25891881-TTAAGAA-T
• MyVariant Identifiers: chr21:g.27264194_27264199del (hg19) ; chr21:g.25891882_25891887del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891882_25891887del , CM000683.2:g.25891882_25891887del	GRCh38
NC_000021.8:g.27264194_27264199del , CM000683.1:g.27264194_27264199del	GRCh37
NC_000021.7:g.26186065_26186070del	NCBI36
NG_007376.1:g.283934_283939del
NG_007376.2:g.284242_284247del

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2032-19_2032-14del
ENST00000707133.1:n.462-19_462-14del
ENST00000707134.1:n.731-19_731-14del
ENST00000346798.8:c.2065-19_2065-14del MANE Select	ENSP00000284981.4:n.2065-19_2065-14del
ENST00000346798.7:c.2065-19_2065-14del	ENSP00000284981.4:n.2065-19_2065-14del
ENST00000348990.9:c.1840-19_1840-14del	ENSP00000345463.5:n.1840-19_1840-14del
ENST00000354192.7:c.1672-19_1672-14del	ENSP00000346129.3:n.1672-19_1672-14del
ENST00000357903.7:c.2008-19_2008-14del	ENSP00000350578.3:n.2008-19_2008-14del
ENST00000358918.7:c.2011-19_2011-14del	ENSP00000351796.3:n.2011-19_2011-14del
ENST00000359726.7:c.1735-19_1735-14del	ENSP00000352760.4:n.1735-19_1735-14del
ENST00000439274.6:c.1897-19_1897-14del	ENSP00000398879.2:n.1897-19_1897-14del
ENST00000440126.7:c.1993-19_1993-14del	ENSP00000387483.2:n.1993-19_1993-14del
ENST00000464867.1:n.412-19_412-14del
NM_000484.3:c.2065-19_2065-14del	NP_000475.1:n.2065-19_2065-14del
NM_001136016.3:c.1993-19_1993-14del	NP_001129488.1:n.1993-19_1993-14del
NM_001136129.2:c.1672-19_1672-14del	NP_001129601.1:n.1672-19_1672-14del
NM_001136130.2:c.1897-19_1897-14del	NP_001129602.1:n.1897-19_1897-14del
NM_001136131.2:c.1735-19_1735-14del	NP_001129603.1:n.1735-19_1735-14del
NM_001204301.1:c.2011-19_2011-14del	NP_001191230.1:n.2011-19_2011-14del
NM_001204302.1:c.1954-19_1954-14del	NP_001191231.1:n.1954-19_1954-14del
NM_001204303.1:c.1786-19_1786-14del	NP_001191232.1:n.1786-19_1786-14del
NM_201413.2:c.2008-19_2008-14del	NP_958816.1:n.2008-19_2008-14del
NM_201414.2:c.1840-19_1840-14del	NP_958817.1:n.1840-19_1840-14del
NM_000484.4:c.2065-19_2065-14del MANE Select	NP_000475.1:n.2065-19_2065-14del
NM_001136129.3:c.1672-19_1672-14del	NP_001129601.1:n.1672-19_1672-14del
NM_001136130.3:c.1897-19_1897-14del	NP_001129602.1:n.1897-19_1897-14del
NM_001204301.2:c.2011-19_2011-14del	NP_001191230.1:n.2011-19_2011-14del
NM_001204302.2:c.1954-19_1954-14del	NP_001191231.1:n.1954-19_1954-14del
NM_001204303.2:c.1786-19_1786-14del	NP_001191232.1:n.1786-19_1786-14del
NM_201413.3:c.2008-19_2008-14del	NP_958816.1:n.2008-19_2008-14del
NM_201414.3:c.1840-19_1840-14del	NP_958817.1:n.1840-19_1840-14del
NM_001136131.3:c.1735-19_1735-14del	NP_001129603.1:n.1735-19_1735-14del
NM_001385253.1:c.1897-19_1897-14del	NP_001372182.1:n.1897-19_1897-14del