Canonical Allele Identifier: CA2383551579
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891679_25891681delinsAGT , CM000683.2:g.25891679_25891681delinsAGT GRCh38
NC_000021.8:g.27263991_27263993delinsAGT , CM000683.1:g.27263991_27263993delinsAGT GRCh37
NC_000021.7:g.26185862_26185864delinsAGT NCBI36
NG_007376.1:g.284140_284142delinsACT
NG_007376.2:g.284448_284450delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2178+41_2178+43delinsACT
ENST00000707133.1:n.608+41_608+43delinsACT
ENST00000707134.1:n.877+41_877+43delinsACT
ENST00000346798.8:c.2211+41_2211+43delinsACT MANE Select ENSP00000284981.4:n.2211+41_2211+43delinsACT
ENST00000346798.7:c.2211+41_2211+43delinsACT ENSP00000284981.4:n.2211+41_2211+43delinsACT
ENST00000348990.9:c.1986+41_1986+43delinsACT ENSP00000345463.5:n.1986+41_1986+43delinsACT
ENST00000354192.7:c.1818+41_1818+43delinsACT ENSP00000346129.3:n.1818+41_1818+43delinsACT
ENST00000357903.7:c.2154+41_2154+43delinsACT ENSP00000350578.3:n.2154+41_2154+43delinsACT
ENST00000358918.7:c.2157+41_2157+43delinsACT ENSP00000351796.3:n.2157+41_2157+43delinsACT
ENST00000359726.7:c.1881+41_1881+43delinsACT ENSP00000352760.4:n.1881+41_1881+43delinsACT
ENST00000439274.6:c.2043+41_2043+43delinsACT ENSP00000398879.2:n.2043+41_2043+43delinsACT
ENST00000440126.7:c.2139+41_2139+43delinsACT ENSP00000387483.2:n.2139+41_2139+43delinsACT
ENST00000464867.1:n.558+41_558+43delinsACT
NM_000484.3:c.2211+41_2211+43delinsACT NP_000475.1:n.2211+41_2211+43delinsACT
NM_001136016.3:c.2139+41_2139+43delinsACT NP_001129488.1:n.2139+41_2139+43delinsACT
NM_001136129.2:c.1818+41_1818+43delinsACT NP_001129601.1:n.1818+41_1818+43delinsACT
NM_001136130.2:c.2043+41_2043+43delinsACT NP_001129602.1:n.2043+41_2043+43delinsACT
NM_001136131.2:c.1881+41_1881+43delinsACT NP_001129603.1:n.1881+41_1881+43delinsACT
NM_001204301.1:c.2157+41_2157+43delinsACT NP_001191230.1:n.2157+41_2157+43delinsACT
NM_001204302.1:c.2100+41_2100+43delinsACT NP_001191231.1:n.2100+41_2100+43delinsACT
NM_001204303.1:c.1932+41_1932+43delinsACT NP_001191232.1:n.1932+41_1932+43delinsACT
NM_201413.2:c.2154+41_2154+43delinsACT NP_958816.1:n.2154+41_2154+43delinsACT
NM_201414.2:c.1986+41_1986+43delinsACT NP_958817.1:n.1986+41_1986+43delinsACT
NM_000484.4:c.2211+41_2211+43delinsACT MANE Select NP_000475.1:n.2211+41_2211+43delinsACT
NM_001136129.3:c.1818+41_1818+43delinsACT NP_001129601.1:n.1818+41_1818+43delinsACT
NM_001136130.3:c.2043+41_2043+43delinsACT NP_001129602.1:n.2043+41_2043+43delinsACT
NM_001204301.2:c.2157+41_2157+43delinsACT NP_001191230.1:n.2157+41_2157+43delinsACT
NM_001204302.2:c.2100+41_2100+43delinsACT NP_001191231.1:n.2100+41_2100+43delinsACT
NM_001204303.2:c.1932+41_1932+43delinsACT NP_001191232.1:n.1932+41_1932+43delinsACT
NM_201413.3:c.2154+41_2154+43delinsACT NP_958816.1:n.2154+41_2154+43delinsACT
NM_201414.3:c.1986+41_1986+43delinsACT NP_958817.1:n.1986+41_1986+43delinsACT
NM_001136131.3:c.1881+41_1881+43delinsACT NP_001129603.1:n.1881+41_1881+43delinsACT
NM_001385253.1:c.2043+41_2043+43delinsACT NP_001372182.1:n.2043+41_2043+43delinsACT