Canonical Allele Identifier: CA9987084
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs768968457

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897566T>C , CM000683.2:g.25897566T>C GRCh38
NC_000021.8:g.27269878T>C , CM000683.1:g.27269878T>C GRCh37
NC_000021.7:g.26191749T>C NCBI36
NG_007376.1:g.278255A>G
NG_007376.2:g.278563A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2031+7A>G
ENST00000707133.1:n.461+7A>G
ENST00000707134.1:n.730+7A>G
ENST00000346798.8:c.2064+7A>G MANE Select ENSP00000284981.4:n.2064+7A>G
ENST00000346798.7:c.2064+7A>G ENSP00000284981.4:n.2064+7A>G
ENST00000348990.9:c.1839+7A>G ENSP00000345463.5:n.1839+7A>G
ENST00000354192.7:c.1671+7A>G ENSP00000346129.3:n.1671+7A>G
ENST00000357903.7:c.2007+7A>G ENSP00000350578.3:n.2007+7A>G
ENST00000358918.7:c.2010+7A>G ENSP00000351796.3:n.2010+7A>G
ENST00000359726.7:c.1734+7A>G ENSP00000352760.4:n.1734+7A>G
ENST00000439274.6:c.1896+7A>G ENSP00000398879.2:n.1896+7A>G
ENST00000440126.7:c.1992+7A>G ENSP00000387483.2:n.1992+7A>G
ENST00000464867.1:n.411+7A>G
NM_000484.3:c.2064+7A>G NP_000475.1:n.2064+7A>G
NM_001136016.3:c.1992+7A>G NP_001129488.1:n.1992+7A>G
NM_001136129.2:c.1671+7A>G NP_001129601.1:n.1671+7A>G
NM_001136130.2:c.1896+7A>G NP_001129602.1:n.1896+7A>G
NM_001136131.2:c.1734+7A>G NP_001129603.1:n.1734+7A>G
NM_001204301.1:c.2010+7A>G NP_001191230.1:n.2010+7A>G
NM_001204302.1:c.1953+7A>G NP_001191231.1:n.1953+7A>G
NM_001204303.1:c.1785+7A>G NP_001191232.1:n.1785+7A>G
NM_201413.2:c.2007+7A>G NP_958816.1:n.2007+7A>G
NM_201414.2:c.1839+7A>G NP_958817.1:n.1839+7A>G
NM_000484.4:c.2064+7A>G MANE Select NP_000475.1:n.2064+7A>G
NM_001136129.3:c.1671+7A>G NP_001129601.1:n.1671+7A>G
NM_001136130.3:c.1896+7A>G NP_001129602.1:n.1896+7A>G
NM_001204301.2:c.2010+7A>G NP_001191230.1:n.2010+7A>G
NM_001204302.2:c.1953+7A>G NP_001191231.1:n.1953+7A>G
NM_001204303.2:c.1785+7A>G NP_001191232.1:n.1785+7A>G
NM_201413.3:c.2007+7A>G NP_958816.1:n.2007+7A>G
NM_201414.3:c.1839+7A>G NP_958817.1:n.1839+7A>G
NM_001136131.3:c.1734+7A>G NP_001129603.1:n.1734+7A>G
NM_001385253.1:c.1896+7A>G NP_001372182.1:n.1896+7A>G