Canonical Allele Identifier: CA1021421975

Gene: APP

Linked Data

• gnomAD v3: 21-25892046-T-TAAAACAAAAAA
• gnomAD v4: 21-25892046-T-TAAAACAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25892050_25892051insCAAAAAAAAAA , CM000683.2:g.25892050_25892051insCAAAAAAAAAA	GRCh38
NC_000021.8:g.27264362_27264363insCAAAAAAAAAA , CM000683.1:g.27264362_27264363insCAAAAAAAAAA	GRCh37
NC_000021.7:g.26186233_26186234insCAAAAAAAAAA	NCBI36
NG_007376.1:g.283774_283775insTTTTTTGTTTT
NG_007376.2:g.284082_284083insTTTTTTGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2032-179_2032-178insTTTTTTGTTTT
ENST00000707133.1:n.462-179_462-178insTTTTTTGTTTT
ENST00000707134.1:n.731-179_731-178insTTTTTTGTTTT
ENST00000346798.8:c.2065-179_2065-178insTTTTTTGTTTT MANE Select	ENSP00000284981.4:n.2065-179_2065-178insTTTTTTGTTTT
ENST00000346798.7:c.2065-179_2065-178insTTTTTTGTTTT	ENSP00000284981.4:n.2065-179_2065-178insTTTTTTGTTTT
ENST00000348990.9:c.1840-179_1840-178insTTTTTTGTTTT	ENSP00000345463.5:n.1840-179_1840-178insTTTTTTGTTTT
ENST00000354192.7:c.1672-179_1672-178insTTTTTTGTTTT	ENSP00000346129.3:n.1672-179_1672-178insTTTTTTGTTTT
ENST00000357903.7:c.2008-179_2008-178insTTTTTTGTTTT	ENSP00000350578.3:n.2008-179_2008-178insTTTTTTGTTTT
ENST00000358918.7:c.2011-179_2011-178insTTTTTTGTTTT	ENSP00000351796.3:n.2011-179_2011-178insTTTTTTGTTTT
ENST00000359726.7:c.1735-179_1735-178insTTTTTTGTTTT	ENSP00000352760.4:n.1735-179_1735-178insTTTTTTGTTTT
ENST00000439274.6:c.1897-179_1897-178insTTTTTTGTTTT	ENSP00000398879.2:n.1897-179_1897-178insTTTTTTGTTTT
ENST00000440126.7:c.1993-179_1993-178insTTTTTTGTTTT	ENSP00000387483.2:n.1993-179_1993-178insTTTTTTGTTTT
ENST00000464867.1:n.412-179_412-178insTTTTTTGTTTT
NM_000484.3:c.2065-179_2065-178insTTTTTTGTTTT	NP_000475.1:n.2065-179_2065-178insTTTTTTGTTTT
NM_001136016.3:c.1993-179_1993-178insTTTTTTGTTTT	NP_001129488.1:n.1993-179_1993-178insTTTTTTGTTTT
NM_001136129.2:c.1672-179_1672-178insTTTTTTGTTTT	NP_001129601.1:n.1672-179_1672-178insTTTTTTGTTTT
NM_001136130.2:c.1897-179_1897-178insTTTTTTGTTTT	NP_001129602.1:n.1897-179_1897-178insTTTTTTGTTTT
NM_001136131.2:c.1735-179_1735-178insTTTTTTGTTTT	NP_001129603.1:n.1735-179_1735-178insTTTTTTGTTTT
NM_001204301.1:c.2011-179_2011-178insTTTTTTGTTTT	NP_001191230.1:n.2011-179_2011-178insTTTTTTGTTTT
NM_001204302.1:c.1954-179_1954-178insTTTTTTGTTTT	NP_001191231.1:n.1954-179_1954-178insTTTTTTGTTTT
NM_001204303.1:c.1786-179_1786-178insTTTTTTGTTTT	NP_001191232.1:n.1786-179_1786-178insTTTTTTGTTTT
NM_201413.2:c.2008-179_2008-178insTTTTTTGTTTT	NP_958816.1:n.2008-179_2008-178insTTTTTTGTTTT
NM_201414.2:c.1840-179_1840-178insTTTTTTGTTTT	NP_958817.1:n.1840-179_1840-178insTTTTTTGTTTT
NM_000484.4:c.2065-179_2065-178insTTTTTTGTTTT MANE Select	NP_000475.1:n.2065-179_2065-178insTTTTTTGTTTT
NM_001136129.3:c.1672-179_1672-178insTTTTTTGTTTT	NP_001129601.1:n.1672-179_1672-178insTTTTTTGTTTT
NM_001136130.3:c.1897-179_1897-178insTTTTTTGTTTT	NP_001129602.1:n.1897-179_1897-178insTTTTTTGTTTT
NM_001204301.2:c.2011-179_2011-178insTTTTTTGTTTT	NP_001191230.1:n.2011-179_2011-178insTTTTTTGTTTT
NM_001204302.2:c.1954-179_1954-178insTTTTTTGTTTT	NP_001191231.1:n.1954-179_1954-178insTTTTTTGTTTT
NM_001204303.2:c.1786-179_1786-178insTTTTTTGTTTT	NP_001191232.1:n.1786-179_1786-178insTTTTTTGTTTT
NM_201413.3:c.2008-179_2008-178insTTTTTTGTTTT	NP_958816.1:n.2008-179_2008-178insTTTTTTGTTTT
NM_201414.3:c.1840-179_1840-178insTTTTTTGTTTT	NP_958817.1:n.1840-179_1840-178insTTTTTTGTTTT
NM_001136131.3:c.1735-179_1735-178insTTTTTTGTTTT	NP_001129603.1:n.1735-179_1735-178insTTTTTTGTTTT
NM_001385253.1:c.1897-179_1897-178insTTTTTTGTTTT	NP_001372182.1:n.1897-179_1897-178insTTTTTTGTTTT