Canonical Allele Identifier: CA2383551964
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25892446_25892447delinsGA , CM000683.2:g.25892446_25892447delinsGA GRCh38
NC_000021.8:g.27264758_27264759delinsGA , CM000683.1:g.27264758_27264759delinsGA GRCh37
NC_000021.7:g.26186629_26186630delinsGA NCBI36
NG_007376.1:g.283374_283375delinsTC
NG_007376.2:g.283682_283683delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2032-579_2032-578delinsTC
ENST00000707133.1:n.462-579_462-578delinsTC
ENST00000707134.1:n.731-579_731-578delinsTC
ENST00000346798.8:c.2065-579_2065-578delinsTC MANE Select ENSP00000284981.4:n.2065-579_2065-578delinsTC
ENST00000346798.7:c.2065-579_2065-578delinsTC ENSP00000284981.4:n.2065-579_2065-578delinsTC
ENST00000348990.9:c.1840-579_1840-578delinsTC ENSP00000345463.5:n.1840-579_1840-578delinsTC
ENST00000354192.7:c.1672-579_1672-578delinsTC ENSP00000346129.3:n.1672-579_1672-578delinsTC
ENST00000357903.7:c.2008-579_2008-578delinsTC ENSP00000350578.3:n.2008-579_2008-578delinsTC
ENST00000358918.7:c.2011-579_2011-578delinsTC ENSP00000351796.3:n.2011-579_2011-578delinsTC
ENST00000359726.7:c.1735-579_1735-578delinsTC ENSP00000352760.4:n.1735-579_1735-578delinsTC
ENST00000439274.6:c.1897-579_1897-578delinsTC ENSP00000398879.2:n.1897-579_1897-578delinsTC
ENST00000440126.7:c.1993-579_1993-578delinsTC ENSP00000387483.2:n.1993-579_1993-578delinsTC
ENST00000464867.1:n.412-579_412-578delinsTC
NM_000484.3:c.2065-579_2065-578delinsTC NP_000475.1:n.2065-579_2065-578delinsTC
NM_001136016.3:c.1993-579_1993-578delinsTC NP_001129488.1:n.1993-579_1993-578delinsTC
NM_001136129.2:c.1672-579_1672-578delinsTC NP_001129601.1:n.1672-579_1672-578delinsTC
NM_001136130.2:c.1897-579_1897-578delinsTC NP_001129602.1:n.1897-579_1897-578delinsTC
NM_001136131.2:c.1735-579_1735-578delinsTC NP_001129603.1:n.1735-579_1735-578delinsTC
NM_001204301.1:c.2011-579_2011-578delinsTC NP_001191230.1:n.2011-579_2011-578delinsTC
NM_001204302.1:c.1954-579_1954-578delinsTC NP_001191231.1:n.1954-579_1954-578delinsTC
NM_001204303.1:c.1786-579_1786-578delinsTC NP_001191232.1:n.1786-579_1786-578delinsTC
NM_201413.2:c.2008-579_2008-578delinsTC NP_958816.1:n.2008-579_2008-578delinsTC
NM_201414.2:c.1840-579_1840-578delinsTC NP_958817.1:n.1840-579_1840-578delinsTC
NM_000484.4:c.2065-579_2065-578delinsTC MANE Select NP_000475.1:n.2065-579_2065-578delinsTC
NM_001136129.3:c.1672-579_1672-578delinsTC NP_001129601.1:n.1672-579_1672-578delinsTC
NM_001136130.3:c.1897-579_1897-578delinsTC NP_001129602.1:n.1897-579_1897-578delinsTC
NM_001204301.2:c.2011-579_2011-578delinsTC NP_001191230.1:n.2011-579_2011-578delinsTC
NM_001204302.2:c.1954-579_1954-578delinsTC NP_001191231.1:n.1954-579_1954-578delinsTC
NM_001204303.2:c.1786-579_1786-578delinsTC NP_001191232.1:n.1786-579_1786-578delinsTC
NM_201413.3:c.2008-579_2008-578delinsTC NP_958816.1:n.2008-579_2008-578delinsTC
NM_201414.3:c.1840-579_1840-578delinsTC NP_958817.1:n.1840-579_1840-578delinsTC
NM_001136131.3:c.1735-579_1735-578delinsTC NP_001129603.1:n.1735-579_1735-578delinsTC
NM_001385253.1:c.1897-579_1897-578delinsTC NP_001372182.1:n.1897-579_1897-578delinsTC