Canonical Allele Identifier: CA409806586
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 2047418
ClinVar RCV Id: RCV002926844
dbSNP Id: rs1305531440

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897668C>T , CM000683.2:g.25897668C>T GRCh38
NC_000021.8:g.27269980C>T , CM000683.1:g.27269980C>T GRCh37
NC_000021.7:g.26191851C>T NCBI36
NG_007376.1:g.278153G>A
NG_007376.2:g.278461G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1936G>A
ENST00000707133.1:n.366G>A
ENST00000707134.1:n.635G>A
ENST00000346798.8:c.1969G>A MANE Select ENSP00000284981.4:p.Gly657Arg
ENST00000346798.7:c.1969G>A ENSP00000284981.4:p.Gly657Arg
ENST00000348990.9:c.1744G>A ENSP00000345463.5:p.Gly582Arg
ENST00000354192.7:c.1576G>A ENSP00000346129.3:p.Gly526Arg
ENST00000357903.7:c.1912G>A ENSP00000350578.3:p.Gly638Arg
ENST00000358918.7:c.1915G>A ENSP00000351796.3:p.Gly639Arg
ENST00000359726.7:c.1639G>A ENSP00000352760.4:p.Gly547Arg
ENST00000439274.6:c.1801G>A ENSP00000398879.2:p.Gly601Arg
ENST00000440126.7:c.1897G>A ENSP00000387483.2:p.Gly633Arg
ENST00000464867.1:n.316G>A
NM_000484.3:c.1969G>A NP_000475.1:p.Gly657Arg
NM_001136016.3:c.1897G>A NP_001129488.1:p.Gly633Arg
NM_001136129.2:c.1576G>A NP_001129601.1:p.Gly526Arg
NM_001136130.2:c.1801G>A NP_001129602.1:p.Gly601Arg
NM_001136131.2:c.1639G>A NP_001129603.1:p.Gly547Arg
NM_001204301.1:c.1915G>A NP_001191230.1:p.Gly639Arg
NM_001204302.1:c.1858G>A NP_001191231.1:p.Gly620Arg
NM_001204303.1:c.1690G>A NP_001191232.1:p.Gly564Arg
NM_201413.2:c.1912G>A NP_958816.1:p.Gly638Arg
NM_201414.2:c.1744G>A NP_958817.1:p.Gly582Arg
NM_000484.4:c.1969G>A MANE Select NP_000475.1:p.Gly657Arg
NM_001136129.3:c.1576G>A NP_001129601.1:p.Gly526Arg
NM_001136130.3:c.1801G>A NP_001129602.1:p.Gly601Arg
NM_001204301.2:c.1915G>A NP_001191230.1:p.Gly639Arg
NM_001204302.2:c.1858G>A NP_001191231.1:p.Gly620Arg
NM_001204303.2:c.1690G>A NP_001191232.1:p.Gly564Arg
NM_201413.3:c.1912G>A NP_958816.1:p.Gly638Arg
NM_201414.3:c.1744G>A NP_958817.1:p.Gly582Arg
NM_001136131.3:c.1639G>A NP_001129603.1:p.Gly547Arg
NM_001385253.1:c.1801G>A NP_001372182.1:p.Gly601Arg