Canonical Allele Identifier: CA409806246
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897581G>A , CM000683.2:g.25897581G>A GRCh38
NC_000021.8:g.27269893G>A , CM000683.1:g.27269893G>A GRCh37
NC_000021.7:g.26191764G>A NCBI36
NG_007376.1:g.278240C>T
NG_007376.2:g.278548C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2023C>T
ENST00000707133.1:n.453C>T
ENST00000707134.1:n.722C>T
ENST00000346798.8:c.2056C>T MANE Select ENSP00000284981.4:p.Gln686Ter
ENST00000346798.7:c.2056C>T ENSP00000284981.4:p.Gln686Ter
ENST00000348990.9:c.1831C>T ENSP00000345463.5:p.Gln611Ter
ENST00000354192.7:c.1663C>T ENSP00000346129.3:p.Gln555Ter
ENST00000357903.7:c.1999C>T ENSP00000350578.3:p.Gln667Ter
ENST00000358918.7:c.2002C>T ENSP00000351796.3:p.Gln668Ter
ENST00000359726.7:c.1726C>T ENSP00000352760.4:p.Gln576Ter
ENST00000439274.6:c.1888C>T ENSP00000398879.2:p.Gln630Ter
ENST00000440126.7:c.1984C>T ENSP00000387483.2:p.Gln662Ter
ENST00000464867.1:n.403C>T
NM_000484.3:c.2056C>T NP_000475.1:p.Gln686Ter
NM_001136016.3:c.1984C>T NP_001129488.1:p.Gln662Ter
NM_001136129.2:c.1663C>T NP_001129601.1:p.Gln555Ter
NM_001136130.2:c.1888C>T NP_001129602.1:p.Gln630Ter
NM_001136131.2:c.1726C>T NP_001129603.1:p.Gln576Ter
NM_001204301.1:c.2002C>T NP_001191230.1:p.Gln668Ter
NM_001204302.1:c.1945C>T NP_001191231.1:p.Gln649Ter
NM_001204303.1:c.1777C>T NP_001191232.1:p.Gln593Ter
NM_201413.2:c.1999C>T NP_958816.1:p.Gln667Ter
NM_201414.2:c.1831C>T NP_958817.1:p.Gln611Ter
NM_000484.4:c.2056C>T MANE Select NP_000475.1:p.Gln686Ter
NM_001136129.3:c.1663C>T NP_001129601.1:p.Gln555Ter
NM_001136130.3:c.1888C>T NP_001129602.1:p.Gln630Ter
NM_001204301.2:c.2002C>T NP_001191230.1:p.Gln668Ter
NM_001204302.2:c.1945C>T NP_001191231.1:p.Gln649Ter
NM_001204303.2:c.1777C>T NP_001191232.1:p.Gln593Ter
NM_201413.3:c.1999C>T NP_958816.1:p.Gln667Ter
NM_201414.3:c.1831C>T NP_958817.1:p.Gln611Ter
NM_001136131.3:c.1726C>T NP_001129603.1:p.Gln576Ter
NM_001385253.1:c.1888C>T NP_001372182.1:p.Gln630Ter