Canonical Allele Identifier: CA1021422044

Gene: APP

Linked Data

• gnomAD v3: 21-25892159-C-CCCT
• gnomAD v4: 21-25892159-C-CCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25892160_25892161insCTC , CM000683.2:g.25892160_25892161insCTC	GRCh38
NC_000021.8:g.27264472_27264473insCTC , CM000683.1:g.27264472_27264473insCTC	GRCh37
NC_000021.7:g.26186343_26186344insCTC	NCBI36
NG_007376.1:g.283661_283662insAGG
NG_007376.2:g.283969_283970insAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2032-292_2032-291insAGG
ENST00000707133.1:n.462-292_462-291insAGG
ENST00000707134.1:n.731-292_731-291insAGG
ENST00000346798.8:c.2065-292_2065-291insAGG MANE Select	ENSP00000284981.4:n.2065-292_2065-291insAGG
ENST00000346798.7:c.2065-292_2065-291insAGG	ENSP00000284981.4:n.2065-292_2065-291insAGG
ENST00000348990.9:c.1840-292_1840-291insAGG	ENSP00000345463.5:n.1840-292_1840-291insAGG
ENST00000354192.7:c.1672-292_1672-291insAGG	ENSP00000346129.3:n.1672-292_1672-291insAGG
ENST00000357903.7:c.2008-292_2008-291insAGG	ENSP00000350578.3:n.2008-292_2008-291insAGG
ENST00000358918.7:c.2011-292_2011-291insAGG	ENSP00000351796.3:n.2011-292_2011-291insAGG
ENST00000359726.7:c.1735-292_1735-291insAGG	ENSP00000352760.4:n.1735-292_1735-291insAGG
ENST00000439274.6:c.1897-292_1897-291insAGG	ENSP00000398879.2:n.1897-292_1897-291insAGG
ENST00000440126.7:c.1993-292_1993-291insAGG	ENSP00000387483.2:n.1993-292_1993-291insAGG
ENST00000464867.1:n.412-292_412-291insAGG
NM_000484.3:c.2065-292_2065-291insAGG	NP_000475.1:n.2065-292_2065-291insAGG
NM_001136016.3:c.1993-292_1993-291insAGG	NP_001129488.1:n.1993-292_1993-291insAGG
NM_001136129.2:c.1672-292_1672-291insAGG	NP_001129601.1:n.1672-292_1672-291insAGG
NM_001136130.2:c.1897-292_1897-291insAGG	NP_001129602.1:n.1897-292_1897-291insAGG
NM_001136131.2:c.1735-292_1735-291insAGG	NP_001129603.1:n.1735-292_1735-291insAGG
NM_001204301.1:c.2011-292_2011-291insAGG	NP_001191230.1:n.2011-292_2011-291insAGG
NM_001204302.1:c.1954-292_1954-291insAGG	NP_001191231.1:n.1954-292_1954-291insAGG
NM_001204303.1:c.1786-292_1786-291insAGG	NP_001191232.1:n.1786-292_1786-291insAGG
NM_201413.2:c.2008-292_2008-291insAGG	NP_958816.1:n.2008-292_2008-291insAGG
NM_201414.2:c.1840-292_1840-291insAGG	NP_958817.1:n.1840-292_1840-291insAGG
NM_000484.4:c.2065-292_2065-291insAGG MANE Select	NP_000475.1:n.2065-292_2065-291insAGG
NM_001136129.3:c.1672-292_1672-291insAGG	NP_001129601.1:n.1672-292_1672-291insAGG
NM_001136130.3:c.1897-292_1897-291insAGG	NP_001129602.1:n.1897-292_1897-291insAGG
NM_001204301.2:c.2011-292_2011-291insAGG	NP_001191230.1:n.2011-292_2011-291insAGG
NM_001204302.2:c.1954-292_1954-291insAGG	NP_001191231.1:n.1954-292_1954-291insAGG
NM_001204303.2:c.1786-292_1786-291insAGG	NP_001191232.1:n.1786-292_1786-291insAGG
NM_201413.3:c.2008-292_2008-291insAGG	NP_958816.1:n.2008-292_2008-291insAGG
NM_201414.3:c.1840-292_1840-291insAGG	NP_958817.1:n.1840-292_1840-291insAGG
NM_001136131.3:c.1735-292_1735-291insAGG	NP_001129603.1:n.1735-292_1735-291insAGG
NM_001385253.1:c.1897-292_1897-291insAGG	NP_001372182.1:n.1897-292_1897-291insAGG