Canonical Allele Identifier: CA2383554876

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897534_25897538delinsGACAA , CM000683.2:g.25897534_25897538delinsGACAA	GRCh38
NC_000021.8:g.27269846_27269850delinsGACAA , CM000683.1:g.27269846_27269850delinsGACAA	GRCh37
NC_000021.7:g.26191717_26191721delinsGACAA	NCBI36
NG_007376.1:g.278283_278287delinsTTGTC
NG_007376.2:g.278591_278595delinsTTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2031+35_2031+39delinsTTGTC
ENST00000707133.1:n.461+35_461+39delinsTTGTC
ENST00000707134.1:n.730+35_730+39delinsTTGTC
ENST00000346798.8:c.2064+35_2064+39delinsTTGTC MANE Select	ENSP00000284981.4:n.2064+35_2064+39delinsTTGTC
ENST00000346798.7:c.2064+35_2064+39delinsTTGTC	ENSP00000284981.4:n.2064+35_2064+39delinsTTGTC
ENST00000348990.9:c.1839+35_1839+39delinsTTGTC	ENSP00000345463.5:n.1839+35_1839+39delinsTTGTC
ENST00000354192.7:c.1671+35_1671+39delinsTTGTC	ENSP00000346129.3:n.1671+35_1671+39delinsTTGTC
ENST00000357903.7:c.2007+35_2007+39delinsTTGTC	ENSP00000350578.3:n.2007+35_2007+39delinsTTGTC
ENST00000358918.7:c.2010+35_2010+39delinsTTGTC	ENSP00000351796.3:n.2010+35_2010+39delinsTTGTC
ENST00000359726.7:c.1734+35_1734+39delinsTTGTC	ENSP00000352760.4:n.1734+35_1734+39delinsTTGTC
ENST00000439274.6:c.1896+35_1896+39delinsTTGTC	ENSP00000398879.2:n.1896+35_1896+39delinsTTGTC
ENST00000440126.7:c.1992+35_1992+39delinsTTGTC	ENSP00000387483.2:n.1992+35_1992+39delinsTTGTC
ENST00000464867.1:n.411+35_411+39delinsTTGTC
NM_000484.3:c.2064+35_2064+39delinsTTGTC	NP_000475.1:n.2064+35_2064+39delinsTTGTC
NM_001136016.3:c.1992+35_1992+39delinsTTGTC	NP_001129488.1:n.1992+35_1992+39delinsTTGTC
NM_001136129.2:c.1671+35_1671+39delinsTTGTC	NP_001129601.1:n.1671+35_1671+39delinsTTGTC
NM_001136130.2:c.1896+35_1896+39delinsTTGTC	NP_001129602.1:n.1896+35_1896+39delinsTTGTC
NM_001136131.2:c.1734+35_1734+39delinsTTGTC	NP_001129603.1:n.1734+35_1734+39delinsTTGTC
NM_001204301.1:c.2010+35_2010+39delinsTTGTC	NP_001191230.1:n.2010+35_2010+39delinsTTGTC
NM_001204302.1:c.1953+35_1953+39delinsTTGTC	NP_001191231.1:n.1953+35_1953+39delinsTTGTC
NM_001204303.1:c.1785+35_1785+39delinsTTGTC	NP_001191232.1:n.1785+35_1785+39delinsTTGTC
NM_201413.2:c.2007+35_2007+39delinsTTGTC	NP_958816.1:n.2007+35_2007+39delinsTTGTC
NM_201414.2:c.1839+35_1839+39delinsTTGTC	NP_958817.1:n.1839+35_1839+39delinsTTGTC
NM_000484.4:c.2064+35_2064+39delinsTTGTC MANE Select	NP_000475.1:n.2064+35_2064+39delinsTTGTC
NM_001136129.3:c.1671+35_1671+39delinsTTGTC	NP_001129601.1:n.1671+35_1671+39delinsTTGTC
NM_001136130.3:c.1896+35_1896+39delinsTTGTC	NP_001129602.1:n.1896+35_1896+39delinsTTGTC
NM_001204301.2:c.2010+35_2010+39delinsTTGTC	NP_001191230.1:n.2010+35_2010+39delinsTTGTC
NM_001204302.2:c.1953+35_1953+39delinsTTGTC	NP_001191231.1:n.1953+35_1953+39delinsTTGTC
NM_001204303.2:c.1785+35_1785+39delinsTTGTC	NP_001191232.1:n.1785+35_1785+39delinsTTGTC
NM_201413.3:c.2007+35_2007+39delinsTTGTC	NP_958816.1:n.2007+35_2007+39delinsTTGTC
NM_201414.3:c.1839+35_1839+39delinsTTGTC	NP_958817.1:n.1839+35_1839+39delinsTTGTC
NM_001136131.3:c.1734+35_1734+39delinsTTGTC	NP_001129603.1:n.1734+35_1734+39delinsTTGTC
NM_001385253.1:c.1896+35_1896+39delinsTTGTC	NP_001372182.1:n.1896+35_1896+39delinsTTGTC