Canonical Allele Identifier: CA319103568
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs890791200

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897656T>C , CM000683.2:g.25897656T>C GRCh38
NC_000021.8:g.27269968T>C , CM000683.1:g.27269968T>C GRCh37
NC_000021.7:g.26191839T>C NCBI36
NG_007376.1:g.278165A>G
NG_007376.2:g.278473A>G

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.1981A>G NP_000475.1:p.Ile661Val
NM_001136016.3:c.1909A>G NP_001129488.1:p.Ile637Val
NM_001136129.2:c.1588A>G NP_001129601.1:p.Ile530Val
NM_001136130.2:c.1813A>G NP_001129602.1:p.Ile605Val
NM_001136131.2:c.1651A>G NP_001129603.1:p.Ile551Val
NM_001204301.1:c.1927A>G NP_001191230.1:p.Ile643Val
NM_001204302.1:c.1870A>G NP_001191231.1:p.Ile624Val
NM_001204303.1:c.1702A>G NP_001191232.1:p.Ile568Val
NM_201413.2:c.1924A>G NP_958816.1:p.Ile642Val
NM_201414.2:c.1756A>G NP_958817.1:p.Ile586Val
NM_000484.4:c.1981A>G MANE Select NP_000475.1:p.Ile661Val
NM_001136129.3:c.1588A>G NP_001129601.1:p.Ile530Val
NM_001136130.3:c.1813A>G NP_001129602.1:p.Ile605Val
NM_001204301.2:c.1927A>G NP_001191230.1:p.Ile643Val
NM_001204302.2:c.1870A>G NP_001191231.1:p.Ile624Val
NM_001204303.2:c.1702A>G NP_001191232.1:p.Ile568Val
NM_201413.3:c.1924A>G NP_958816.1:p.Ile642Val
NM_201414.3:c.1756A>G NP_958817.1:p.Ile586Val
NM_001136131.3:c.1651A>G NP_001129603.1:p.Ile551Val
NM_001385253.1:c.1813A>G NP_001372182.1:p.Ile605Val
ENST00000346798.7:c.1981A>G ENSP00000284981.4:p.Ile661Val
ENST00000348990.9:c.1756A>G ENSP00000345463.5:p.Ile586Val
ENST00000354192.7:c.1588A>G ENSP00000346129.3:p.Ile530Val
ENST00000357903.7:c.1924A>G ENSP00000350578.3:p.Ile642Val
ENST00000358918.7:c.1927A>G ENSP00000351796.3:p.Ile643Val
ENST00000359726.7:c.1651A>G ENSP00000352760.4:p.Ile551Val
ENST00000439274.6:c.1813A>G ENSP00000398879.2:p.Ile605Val
ENST00000440126.7:c.1909A>G ENSP00000387483.2:p.Ile637Val
ENST00000464867.1:n.328A>G