Canonical Allele Identifier: CA409806584
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1936G>T
ENST00000707133.1:n.366G>T
ENST00000707134.1:n.635G>T
ENST00000346798.8:c.1969G>T MANE Select ENSP00000284981.4:p.Gly657Trp
ENST00000346798.7:c.1969G>T ENSP00000284981.4:p.Gly657Trp
ENST00000348990.9:c.1744G>T ENSP00000345463.5:p.Gly582Trp
ENST00000354192.7:c.1576G>T ENSP00000346129.3:p.Gly526Trp
ENST00000357903.7:c.1912G>T ENSP00000350578.3:p.Gly638Trp
ENST00000358918.7:c.1915G>T ENSP00000351796.3:p.Gly639Trp
ENST00000359726.7:c.1639G>T ENSP00000352760.4:p.Gly547Trp
ENST00000439274.6:c.1801G>T ENSP00000398879.2:p.Gly601Trp
ENST00000440126.7:c.1897G>T ENSP00000387483.2:p.Gly633Trp
ENST00000464867.1:n.316G>T
NM_000484.3:c.1969G>T NP_000475.1:p.Gly657Trp
NM_001136016.3:c.1897G>T NP_001129488.1:p.Gly633Trp
NM_001136129.2:c.1576G>T NP_001129601.1:p.Gly526Trp
NM_001136130.2:c.1801G>T NP_001129602.1:p.Gly601Trp
NM_001136131.2:c.1639G>T NP_001129603.1:p.Gly547Trp
NM_001204301.1:c.1915G>T NP_001191230.1:p.Gly639Trp
NM_001204302.1:c.1858G>T NP_001191231.1:p.Gly620Trp
NM_001204303.1:c.1690G>T NP_001191232.1:p.Gly564Trp
NM_201413.2:c.1912G>T NP_958816.1:p.Gly638Trp
NM_201414.2:c.1744G>T NP_958817.1:p.Gly582Trp
NM_000484.4:c.1969G>T MANE Select NP_000475.1:p.Gly657Trp
NM_001136129.3:c.1576G>T NP_001129601.1:p.Gly526Trp
NM_001136130.3:c.1801G>T NP_001129602.1:p.Gly601Trp
NM_001204301.2:c.1915G>T NP_001191230.1:p.Gly639Trp
NM_001204302.2:c.1858G>T NP_001191231.1:p.Gly620Trp
NM_001204303.2:c.1690G>T NP_001191232.1:p.Gly564Trp
NM_201413.3:c.1912G>T NP_958816.1:p.Gly638Trp
NM_201414.3:c.1744G>T NP_958817.1:p.Gly582Trp
NM_001136131.3:c.1639G>T NP_001129603.1:p.Gly547Trp
NM_001385253.1:c.1801G>T NP_001372182.1:p.Gly601Trp