Canonical Allele Identifier: CA2383551567
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891664_25891665delinsGC , CM000683.2:g.25891664_25891665delinsGC GRCh38
NC_000021.8:g.27263976_27263977delinsGC , CM000683.1:g.27263976_27263977delinsGC GRCh37
NC_000021.7:g.26185847_26185848delinsGC NCBI36
NG_007376.1:g.284156_284157delinsGC
NG_007376.2:g.284464_284465delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2178+57_2178+58delinsGC
ENST00000707133.1:n.608+57_608+58delinsGC
ENST00000707134.1:n.877+57_877+58delinsGC
ENST00000346798.8:c.2211+57_2211+58delinsGC MANE Select ENSP00000284981.4:n.2211+57_2211+58delins...
ENST00000346798.7:c.2211+57_2211+58delinsGC ENSP00000284981.4:n.2211+57_2211+58delins...
ENST00000348990.9:c.1986+57_1986+58delinsGC ENSP00000345463.5:n.1986+57_1986+58delins...
ENST00000354192.7:c.1818+57_1818+58delinsGC ENSP00000346129.3:n.1818+57_1818+58delins...
ENST00000357903.7:c.2154+57_2154+58delinsGC ENSP00000350578.3:n.2154+57_2154+58delins...
ENST00000358918.7:c.2157+57_2157+58delinsGC ENSP00000351796.3:n.2157+57_2157+58delins...
ENST00000359726.7:c.1881+57_1881+58delinsGC ENSP00000352760.4:n.1881+57_1881+58delins...
ENST00000439274.6:c.2043+57_2043+58delinsGC ENSP00000398879.2:n.2043+57_2043+58delins...
ENST00000440126.7:c.2139+57_2139+58delinsGC ENSP00000387483.2:n.2139+57_2139+58delins...
ENST00000464867.1:n.558+57_558+58delinsGC
NM_000484.3:c.2211+57_2211+58delinsGC NP_000475.1:n.2211+57_2211+58delinsGC
NM_001136016.3:c.2139+57_2139+58delinsGC NP_001129488.1:n.2139+57_2139+58delinsGC
NM_001136129.2:c.1818+57_1818+58delinsGC NP_001129601.1:n.1818+57_1818+58delinsGC
NM_001136130.2:c.2043+57_2043+58delinsGC NP_001129602.1:n.2043+57_2043+58delinsGC
NM_001136131.2:c.1881+57_1881+58delinsGC NP_001129603.1:n.1881+57_1881+58delinsGC
NM_001204301.1:c.2157+57_2157+58delinsGC NP_001191230.1:n.2157+57_2157+58delinsGC
NM_001204302.1:c.2100+57_2100+58delinsGC NP_001191231.1:n.2100+57_2100+58delinsGC
NM_001204303.1:c.1932+57_1932+58delinsGC NP_001191232.1:n.1932+57_1932+58delinsGC
NM_201413.2:c.2154+57_2154+58delinsGC NP_958816.1:n.2154+57_2154+58delinsGC
NM_201414.2:c.1986+57_1986+58delinsGC NP_958817.1:n.1986+57_1986+58delinsGC
NM_000484.4:c.2211+57_2211+58delinsGC MANE Select NP_000475.1:n.2211+57_2211+58delinsGC
NM_001136129.3:c.1818+57_1818+58delinsGC NP_001129601.1:n.1818+57_1818+58delinsGC
NM_001136130.3:c.2043+57_2043+58delinsGC NP_001129602.1:n.2043+57_2043+58delinsGC
NM_001204301.2:c.2157+57_2157+58delinsGC NP_001191230.1:n.2157+57_2157+58delinsGC
NM_001204302.2:c.2100+57_2100+58delinsGC NP_001191231.1:n.2100+57_2100+58delinsGC
NM_001204303.2:c.1932+57_1932+58delinsGC NP_001191232.1:n.1932+57_1932+58delinsGC
NM_201413.3:c.2154+57_2154+58delinsGC NP_958816.1:n.2154+57_2154+58delinsGC
NM_201414.3:c.1986+57_1986+58delinsGC NP_958817.1:n.1986+57_1986+58delinsGC
NM_001136131.3:c.1881+57_1881+58delinsGC NP_001129603.1:n.1881+57_1881+58delinsGC
NM_001385253.1:c.2043+57_2043+58delinsGC NP_001372182.1:n.2043+57_2043+58delinsGC