Canonical Allele Identifier: CA2383554945
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897649_25897655delinsGTCTTGA , CM000683.2:g.25897649_25897655delinsGTCTTGA GRCh38
NC_000021.8:g.27269961_27269967delinsGTCTTGA , CM000683.1:g.27269961_27269967delinsGTCTTGA GRCh37
NC_000021.7:g.26191832_26191838delinsGTCTTGA NCBI36
NG_007376.1:g.278166_278172delinsTCAAGAC
NG_007376.2:g.278474_278480delinsTCAAGAC

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1949_1955delinsTCAAGAC
ENST00000707133.1:n.379_385delinsTCAAGAC
ENST00000707134.1:n.648_654delinsTCAAGAC
ENST00000346798.8:c.1982_1988delinsTCAAGAC MANE Select ENSP00000284981.4:p.Ile661=
ENST00000346798.7:c.1982_1988delinsTCAAGAC ENSP00000284981.4:p.Ile661=
ENST00000348990.9:c.1757_1763delinsTCAAGAC ENSP00000345463.5:p.Ile586=
ENST00000354192.7:c.1589_1595delinsTCAAGAC ENSP00000346129.3:p.Ile530=
ENST00000357903.7:c.1925_1931delinsTCAAGAC ENSP00000350578.3:p.Ile642=
ENST00000358918.7:c.1928_1934delinsTCAAGAC ENSP00000351796.3:p.Ile643=
ENST00000359726.7:c.1652_1658delinsTCAAGAC ENSP00000352760.4:p.Ile551=
ENST00000439274.6:c.1814_1820delinsTCAAGAC ENSP00000398879.2:p.Ile605=
ENST00000440126.7:c.1910_1916delinsTCAAGAC ENSP00000387483.2:p.Ile637=
ENST00000464867.1:n.329_335delinsTCAAGAC
NM_000484.3:c.1982_1988delinsTCAAGAC NP_000475.1:p.Ile661=
NM_001136016.3:c.1910_1916delinsTCAAGAC NP_001129488.1:p.Ile637=
NM_001136129.2:c.1589_1595delinsTCAAGAC NP_001129601.1:p.Ile530=
NM_001136130.2:c.1814_1820delinsTCAAGAC NP_001129602.1:p.Ile605=
NM_001136131.2:c.1652_1658delinsTCAAGAC NP_001129603.1:p.Ile551=
NM_001204301.1:c.1928_1934delinsTCAAGAC NP_001191230.1:p.Ile643=
NM_001204302.1:c.1871_1877delinsTCAAGAC NP_001191231.1:p.Ile624=
NM_001204303.1:c.1703_1709delinsTCAAGAC NP_001191232.1:p.Ile568=
NM_201413.2:c.1925_1931delinsTCAAGAC NP_958816.1:p.Ile642=
NM_201414.2:c.1757_1763delinsTCAAGAC NP_958817.1:p.Ile586=
NM_000484.4:c.1982_1988delinsTCAAGAC MANE Select NP_000475.1:p.Ile661=
NM_001136129.3:c.1589_1595delinsTCAAGAC NP_001129601.1:p.Ile530=
NM_001136130.3:c.1814_1820delinsTCAAGAC NP_001129602.1:p.Ile605=
NM_001204301.2:c.1928_1934delinsTCAAGAC NP_001191230.1:p.Ile643=
NM_001204302.2:c.1871_1877delinsTCAAGAC NP_001191231.1:p.Ile624=
NM_001204303.2:c.1703_1709delinsTCAAGAC NP_001191232.1:p.Ile568=
NM_201413.3:c.1925_1931delinsTCAAGAC NP_958816.1:p.Ile642=
NM_201414.3:c.1757_1763delinsTCAAGAC NP_958817.1:p.Ile586=
NM_001136131.3:c.1652_1658delinsTCAAGAC NP_001129603.1:p.Ile551=
NM_001385253.1:c.1814_1820delinsTCAAGAC NP_001372182.1:p.Ile605=