Canonical Allele Identifier: CA1021421352
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891411_25891420dup , CM000683.2:g.25891411_25891420dup GRCh38
NC_000021.8:g.27263723_27263732dup , CM000683.1:g.27263723_27263732dup GRCh37
NC_000021.7:g.26185594_26185603dup NCBI36
NG_007376.1:g.284401_284410dup
NG_007376.2:g.284709_284718dup

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2178+302_2178+311dup
ENST00000707133.1:n.608+302_608+311dup
ENST00000707134.1:n.877+302_877+311dup
ENST00000346798.8:c.2211+302_2211+311dup MANE Select ENSP00000284981.4:n.2211+302_2211+311dup
ENST00000346798.7:c.2211+302_2211+311dup ENSP00000284981.4:n.2211+302_2211+311dup
ENST00000348990.9:c.1986+302_1986+311dup ENSP00000345463.5:n.1986+302_1986+311dup
ENST00000354192.7:c.1818+302_1818+311dup ENSP00000346129.3:n.1818+302_1818+311dup
ENST00000357903.7:c.2154+302_2154+311dup ENSP00000350578.3:n.2154+302_2154+311dup
ENST00000358918.7:c.2157+302_2157+311dup ENSP00000351796.3:n.2157+302_2157+311dup
ENST00000359726.7:c.1881+302_1881+311dup ENSP00000352760.4:n.1881+302_1881+311dup
ENST00000439274.6:c.2043+302_2043+311dup ENSP00000398879.2:n.2043+302_2043+311dup
ENST00000440126.7:c.2139+302_2139+311dup ENSP00000387483.2:n.2139+302_2139+311dup
ENST00000464867.1:n.558+302_558+311dup
NM_000484.3:c.2211+302_2211+311dup NP_000475.1:n.2211+302_2211+311dup
NM_001136016.3:c.2139+302_2139+311dup NP_001129488.1:n.2139+302_2139+311dup
NM_001136129.2:c.1818+302_1818+311dup NP_001129601.1:n.1818+302_1818+311dup
NM_001136130.2:c.2043+302_2043+311dup NP_001129602.1:n.2043+302_2043+311dup
NM_001136131.2:c.1881+302_1881+311dup NP_001129603.1:n.1881+302_1881+311dup
NM_001204301.1:c.2157+302_2157+311dup NP_001191230.1:n.2157+302_2157+311dup
NM_001204302.1:c.2100+302_2100+311dup NP_001191231.1:n.2100+302_2100+311dup
NM_001204303.1:c.1932+302_1932+311dup NP_001191232.1:n.1932+302_1932+311dup
NM_201413.2:c.2154+302_2154+311dup NP_958816.1:n.2154+302_2154+311dup
NM_201414.2:c.1986+302_1986+311dup NP_958817.1:n.1986+302_1986+311dup
NM_000484.4:c.2211+302_2211+311dup MANE Select NP_000475.1:n.2211+302_2211+311dup
NM_001136129.3:c.1818+302_1818+311dup NP_001129601.1:n.1818+302_1818+311dup
NM_001136130.3:c.2043+302_2043+311dup NP_001129602.1:n.2043+302_2043+311dup
NM_001204301.2:c.2157+302_2157+311dup NP_001191230.1:n.2157+302_2157+311dup
NM_001204302.2:c.2100+302_2100+311dup NP_001191231.1:n.2100+302_2100+311dup
NM_001204303.2:c.1932+302_1932+311dup NP_001191232.1:n.1932+302_1932+311dup
NM_201413.3:c.2154+302_2154+311dup NP_958816.1:n.2154+302_2154+311dup
NM_201414.3:c.1986+302_1986+311dup NP_958817.1:n.1986+302_1986+311dup
NM_001136131.3:c.1881+302_1881+311dup NP_001129603.1:n.1881+302_1881+311dup
NM_001385253.1:c.2043+302_2043+311dup NP_001372182.1:n.2043+302_2043+311dup