Canonical Allele Identifier: CA2383551463
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891470_25891471delinsAT , CM000683.2:g.25891470_25891471delinsAT GRCh38
NC_000021.8:g.27263782_27263783delinsAT , CM000683.1:g.27263782_27263783delinsAT GRCh37
NC_000021.7:g.26185653_26185654delinsAT NCBI36
NG_007376.1:g.284350_284351delinsAT
NG_007376.2:g.284658_284659delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2178+251_2178+252delinsAT
ENST00000707133.1:n.608+251_608+252delinsAT
ENST00000707134.1:n.877+251_877+252delinsAT
ENST00000346798.8:c.2211+251_2211+252delinsAT MANE Select ENSP00000284981.4:n.2211+251_2211+252deli...
ENST00000346798.7:c.2211+251_2211+252delinsAT ENSP00000284981.4:n.2211+251_2211+252deli...
ENST00000348990.9:c.1986+251_1986+252delinsAT ENSP00000345463.5:n.1986+251_1986+252deli...
ENST00000354192.7:c.1818+251_1818+252delinsAT ENSP00000346129.3:n.1818+251_1818+252deli...
ENST00000357903.7:c.2154+251_2154+252delinsAT ENSP00000350578.3:n.2154+251_2154+252deli...
ENST00000358918.7:c.2157+251_2157+252delinsAT ENSP00000351796.3:n.2157+251_2157+252deli...
ENST00000359726.7:c.1881+251_1881+252delinsAT ENSP00000352760.4:n.1881+251_1881+252deli...
ENST00000439274.6:c.2043+251_2043+252delinsAT ENSP00000398879.2:n.2043+251_2043+252deli...
ENST00000440126.7:c.2139+251_2139+252delinsAT ENSP00000387483.2:n.2139+251_2139+252deli...
ENST00000464867.1:n.558+251_558+252delinsAT
NM_000484.3:c.2211+251_2211+252delinsAT NP_000475.1:n.2211+251_2211+252delinsAT
NM_001136016.3:c.2139+251_2139+252delinsAT NP_001129488.1:n.2139+251_2139+252delinsA...
NM_001136129.2:c.1818+251_1818+252delinsAT NP_001129601.1:n.1818+251_1818+252delinsA...
NM_001136130.2:c.2043+251_2043+252delinsAT NP_001129602.1:n.2043+251_2043+252delinsA...
NM_001136131.2:c.1881+251_1881+252delinsAT NP_001129603.1:n.1881+251_1881+252delinsA...
NM_001204301.1:c.2157+251_2157+252delinsAT NP_001191230.1:n.2157+251_2157+252delinsA...
NM_001204302.1:c.2100+251_2100+252delinsAT NP_001191231.1:n.2100+251_2100+252delinsA...
NM_001204303.1:c.1932+251_1932+252delinsAT NP_001191232.1:n.1932+251_1932+252delinsA...
NM_201413.2:c.2154+251_2154+252delinsAT NP_958816.1:n.2154+251_2154+252delinsAT
NM_201414.2:c.1986+251_1986+252delinsAT NP_958817.1:n.1986+251_1986+252delinsAT
NM_000484.4:c.2211+251_2211+252delinsAT MANE Select NP_000475.1:n.2211+251_2211+252delinsAT
NM_001136129.3:c.1818+251_1818+252delinsAT NP_001129601.1:n.1818+251_1818+252delinsA...
NM_001136130.3:c.2043+251_2043+252delinsAT NP_001129602.1:n.2043+251_2043+252delinsA...
NM_001204301.2:c.2157+251_2157+252delinsAT NP_001191230.1:n.2157+251_2157+252delinsA...
NM_001204302.2:c.2100+251_2100+252delinsAT NP_001191231.1:n.2100+251_2100+252delinsA...
NM_001204303.2:c.1932+251_1932+252delinsAT NP_001191232.1:n.1932+251_1932+252delinsA...
NM_201413.3:c.2154+251_2154+252delinsAT NP_958816.1:n.2154+251_2154+252delinsAT
NM_201414.3:c.1986+251_1986+252delinsAT NP_958817.1:n.1986+251_1986+252delinsAT
NM_001136131.3:c.1881+251_1881+252delinsAT NP_001129603.1:n.1881+251_1881+252delinsA...
NM_001385253.1:c.2043+251_2043+252delinsAT NP_001372182.1:n.2043+251_2043+252delinsA...