Canonical Allele Identifier: CA511686138
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs1452214524

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897579T>C , CM000683.2:g.25897579T>C GRCh38
NC_000021.8:g.27269891T>C , CM000683.1:g.27269891T>C GRCh37
NC_000021.7:g.26191762T>C NCBI36
NG_007376.1:g.278242A>G
NG_007376.2:g.278550A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2025A>G
ENST00000707133.1:n.455A>G
ENST00000707134.1:n.724A>G
ENST00000346798.8:c.2058A>G MANE Select ENSP00000284981.4:p.Gln686=
ENST00000346798.7:c.2058A>G ENSP00000284981.4:p.Gln686=
ENST00000348990.9:c.1833A>G ENSP00000345463.5:p.Gln611=
ENST00000354192.7:c.1665A>G ENSP00000346129.3:p.Gln555=
ENST00000357903.7:c.2001A>G ENSP00000350578.3:p.Gln667=
ENST00000358918.7:c.2004A>G ENSP00000351796.3:p.Gln668=
ENST00000359726.7:c.1728A>G ENSP00000352760.4:p.Gln576=
ENST00000439274.6:c.1890A>G ENSP00000398879.2:p.Gln630=
ENST00000440126.7:c.1986A>G ENSP00000387483.2:p.Gln662=
ENST00000464867.1:n.405A>G
NM_000484.3:c.2058A>G NP_000475.1:p.Gln686=
NM_001136016.3:c.1986A>G NP_001129488.1:p.Gln662=
NM_001136129.2:c.1665A>G NP_001129601.1:p.Gln555=
NM_001136130.2:c.1890A>G NP_001129602.1:p.Gln630=
NM_001136131.2:c.1728A>G NP_001129603.1:p.Gln576=
NM_001204301.1:c.2004A>G NP_001191230.1:p.Gln668=
NM_001204302.1:c.1947A>G NP_001191231.1:p.Gln649=
NM_001204303.1:c.1779A>G NP_001191232.1:p.Gln593=
NM_201413.2:c.2001A>G NP_958816.1:p.Gln667=
NM_201414.2:c.1833A>G NP_958817.1:p.Gln611=
NM_000484.4:c.2058A>G MANE Select NP_000475.1:p.Gln686=
NM_001136129.3:c.1665A>G NP_001129601.1:p.Gln555=
NM_001136130.3:c.1890A>G NP_001129602.1:p.Gln630=
NM_001204301.2:c.2004A>G NP_001191230.1:p.Gln668=
NM_001204302.2:c.1947A>G NP_001191231.1:p.Gln649=
NM_001204303.2:c.1779A>G NP_001191232.1:p.Gln593=
NM_201413.3:c.2001A>G NP_958816.1:p.Gln667=
NM_201414.3:c.1833A>G NP_958817.1:p.Gln611=
NM_001136131.3:c.1728A>G NP_001129603.1:p.Gln576=
NM_001385253.1:c.1890A>G NP_001372182.1:p.Gln630=