Canonical Allele Identifier: CA748247763
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs759980555

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897646_25897648dup , CM000683.2:g.25897646_25897648dup GRCh38
NC_000021.8:g.27269958_27269960dup , CM000683.1:g.27269958_27269960dup GRCh37
NC_000021.7:g.26191829_26191831dup NCBI36
NG_007376.1:g.278177_278179dup
NG_007376.2:g.278485_278487dup

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1960_1962dup
ENST00000707133.1:n.390_392dup
ENST00000707134.1:n.659_661dup
ENST00000346798.8:c.1993_1995dup MANE Select ENSP00000284981.4:p.Glu665_Ile666insGlu
ENST00000346798.7:c.1993_1995dup ENSP00000284981.4:p.Glu665_Ile666insGlu
ENST00000348990.9:c.1768_1770dup ENSP00000345463.5:p.Glu590_Ile591insGlu
ENST00000354192.7:c.1600_1602dup ENSP00000346129.3:p.Glu534_Ile535insGlu
ENST00000357903.7:c.1936_1938dup ENSP00000350578.3:p.Glu646_Ile647insGlu
ENST00000358918.7:c.1939_1941dup ENSP00000351796.3:p.Glu647_Ile648insGlu
ENST00000359726.7:c.1663_1665dup ENSP00000352760.4:p.Glu555_Ile556insGlu
ENST00000439274.6:c.1825_1827dup ENSP00000398879.2:p.Glu609_Ile610insGlu
ENST00000440126.7:c.1921_1923dup ENSP00000387483.2:p.Glu641_Ile642insGlu
ENST00000464867.1:n.340_342dup
NM_000484.3:c.1993_1995dup NP_000475.1:p.Glu665_Ile666insGlu
NM_001136016.3:c.1921_1923dup NP_001129488.1:p.Glu641_Ile642insGlu
NM_001136129.2:c.1600_1602dup NP_001129601.1:p.Glu534_Ile535insGlu
NM_001136130.2:c.1825_1827dup NP_001129602.1:p.Glu609_Ile610insGlu
NM_001136131.2:c.1663_1665dup NP_001129603.1:p.Glu555_Ile556insGlu
NM_001204301.1:c.1939_1941dup NP_001191230.1:p.Glu647_Ile648insGlu
NM_001204302.1:c.1882_1884dup NP_001191231.1:p.Glu628_Ile629insGlu
NM_001204303.1:c.1714_1716dup NP_001191232.1:p.Glu572_Ile573insGlu
NM_201413.2:c.1936_1938dup NP_958816.1:p.Glu646_Ile647insGlu
NM_201414.2:c.1768_1770dup NP_958817.1:p.Glu590_Ile591insGlu
NM_000484.4:c.1993_1995dup MANE Select NP_000475.1:p.Glu665_Ile666insGlu
NM_001136129.3:c.1600_1602dup NP_001129601.1:p.Glu534_Ile535insGlu
NM_001136130.3:c.1825_1827dup NP_001129602.1:p.Glu609_Ile610insGlu
NM_001204301.2:c.1939_1941dup NP_001191230.1:p.Glu647_Ile648insGlu
NM_001204302.2:c.1882_1884dup NP_001191231.1:p.Glu628_Ile629insGlu
NM_001204303.2:c.1714_1716dup NP_001191232.1:p.Glu572_Ile573insGlu
NM_201413.3:c.1936_1938dup NP_958816.1:p.Glu646_Ile647insGlu
NM_201414.3:c.1768_1770dup NP_958817.1:p.Glu590_Ile591insGlu
NM_001136131.3:c.1663_1665dup NP_001129603.1:p.Glu555_Ile556insGlu
NM_001385253.1:c.1825_1827dup NP_001372182.1:p.Glu609_Ile610insGlu