Canonical Allele Identifier: CA2383554791
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897376_25897377delinsAG , CM000683.2:g.25897376_25897377delinsAG GRCh38
NC_000021.8:g.27269688_27269689delinsAG , CM000683.1:g.27269688_27269689delinsAG GRCh37
NC_000021.7:g.26191559_26191560delinsAG NCBI36
NG_007376.1:g.278444_278445delinsCT
NG_007376.2:g.278752_278753delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2031+196_2031+197delinsCT
ENST00000707133.1:n.461+196_461+197delinsCT
ENST00000707134.1:n.730+196_730+197delinsCT
ENST00000346798.8:c.2064+196_2064+197delinsCT MANE Select ENSP00000284981.4:n.2064+196_2064+197delinsCT
ENST00000346798.7:c.2064+196_2064+197delinsCT ENSP00000284981.4:n.2064+196_2064+197delinsCT
ENST00000348990.9:c.1839+196_1839+197delinsCT ENSP00000345463.5:n.1839+196_1839+197delinsCT
ENST00000354192.7:c.1671+196_1671+197delinsCT ENSP00000346129.3:n.1671+196_1671+197delinsCT
ENST00000357903.7:c.2007+196_2007+197delinsCT ENSP00000350578.3:n.2007+196_2007+197delinsCT
ENST00000358918.7:c.2010+196_2010+197delinsCT ENSP00000351796.3:n.2010+196_2010+197delinsCT
ENST00000359726.7:c.1734+196_1734+197delinsCT ENSP00000352760.4:n.1734+196_1734+197delinsCT
ENST00000439274.6:c.1896+196_1896+197delinsCT ENSP00000398879.2:n.1896+196_1896+197delinsCT
ENST00000440126.7:c.1992+196_1992+197delinsCT ENSP00000387483.2:n.1992+196_1992+197delinsCT
ENST00000464867.1:n.411+196_411+197delinsCT
NM_000484.3:c.2064+196_2064+197delinsCT NP_000475.1:n.2064+196_2064+197delinsCT
NM_001136016.3:c.1992+196_1992+197delinsCT NP_001129488.1:n.1992+196_1992+197delinsCT
NM_001136129.2:c.1671+196_1671+197delinsCT NP_001129601.1:n.1671+196_1671+197delinsCT
NM_001136130.2:c.1896+196_1896+197delinsCT NP_001129602.1:n.1896+196_1896+197delinsCT
NM_001136131.2:c.1734+196_1734+197delinsCT NP_001129603.1:n.1734+196_1734+197delinsCT
NM_001204301.1:c.2010+196_2010+197delinsCT NP_001191230.1:n.2010+196_2010+197delinsCT
NM_001204302.1:c.1953+196_1953+197delinsCT NP_001191231.1:n.1953+196_1953+197delinsCT
NM_001204303.1:c.1785+196_1785+197delinsCT NP_001191232.1:n.1785+196_1785+197delinsCT
NM_201413.2:c.2007+196_2007+197delinsCT NP_958816.1:n.2007+196_2007+197delinsCT
NM_201414.2:c.1839+196_1839+197delinsCT NP_958817.1:n.1839+196_1839+197delinsCT
NM_000484.4:c.2064+196_2064+197delinsCT MANE Select NP_000475.1:n.2064+196_2064+197delinsCT
NM_001136129.3:c.1671+196_1671+197delinsCT NP_001129601.1:n.1671+196_1671+197delinsCT
NM_001136130.3:c.1896+196_1896+197delinsCT NP_001129602.1:n.1896+196_1896+197delinsCT
NM_001204301.2:c.2010+196_2010+197delinsCT NP_001191230.1:n.2010+196_2010+197delinsCT
NM_001204302.2:c.1953+196_1953+197delinsCT NP_001191231.1:n.1953+196_1953+197delinsCT
NM_001204303.2:c.1785+196_1785+197delinsCT NP_001191232.1:n.1785+196_1785+197delinsCT
NM_201413.3:c.2007+196_2007+197delinsCT NP_958816.1:n.2007+196_2007+197delinsCT
NM_201414.3:c.1839+196_1839+197delinsCT NP_958817.1:n.1839+196_1839+197delinsCT
NM_001136131.3:c.1734+196_1734+197delinsCT NP_001129603.1:n.1734+196_1734+197delinsCT
NM_001385253.1:c.1896+196_1896+197delinsCT NP_001372182.1:n.1896+196_1896+197delinsCT