Canonical Allele Identifier: CA127802
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18099
dbSNP Id: rs63750579

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891856C>T , CM000683.2:g.25891856C>T GRCh38
NC_000021.8:g.27264168C>T , CM000683.1:g.27264168C>T GRCh37
NC_000021.7:g.26186039C>T NCBI36
NG_007376.1:g.283965G>A
NG_007376.2:g.284273G>A

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2077G>A NP_000475.1:p.Glu693Lys
NM_001136016.3:c.2005G>A NP_001129488.1:p.Glu669Lys
NM_001136129.2:c.1684G>A NP_001129601.1:p.Glu562Lys
NM_001136130.2:c.1909G>A NP_001129602.1:p.Glu637Lys
NM_001136131.2:c.1747G>A NP_001129603.1:p.Glu583Lys
NM_001204301.1:c.2023G>A NP_001191230.1:p.Glu675Lys
NM_001204302.1:c.1966G>A NP_001191231.1:p.Glu656Lys
NM_001204303.1:c.1798G>A NP_001191232.1:p.Glu600Lys
NM_201413.2:c.2020G>A NP_958816.1:p.Glu674Lys
NM_201414.2:c.1852G>A NP_958817.1:p.Glu618Lys
NM_000484.4:c.2077G>A MANE Select NP_000475.1:p.Glu693Lys
NM_001136129.3:c.1684G>A NP_001129601.1:p.Glu562Lys
NM_001136130.3:c.1909G>A NP_001129602.1:p.Glu637Lys
NM_001204301.2:c.2023G>A NP_001191230.1:p.Glu675Lys
NM_001204302.2:c.1966G>A NP_001191231.1:p.Glu656Lys
NM_001204303.2:c.1798G>A NP_001191232.1:p.Glu600Lys
NM_201413.3:c.2020G>A NP_958816.1:p.Glu674Lys
NM_201414.3:c.1852G>A NP_958817.1:p.Glu618Lys
NM_001136131.3:c.1747G>A NP_001129603.1:p.Glu583Lys
NM_001385253.1:c.1909G>A NP_001372182.1:p.Glu637Lys
ENST00000346798.7:c.2077G>A ENSP00000284981.4:p.Glu693Lys
ENST00000348990.9:c.1852G>A ENSP00000345463.5:p.Glu618Lys
ENST00000354192.7:c.1684G>A ENSP00000346129.3:p.Glu562Lys
ENST00000357903.7:c.2020G>A ENSP00000350578.3:p.Glu674Lys
ENST00000358918.7:c.2023G>A ENSP00000351796.3:p.Glu675Lys
ENST00000359726.7:c.1747G>A ENSP00000352760.4:p.Glu583Lys
ENST00000439274.6:c.1909G>A ENSP00000398879.2:p.Glu637Lys
ENST00000440126.7:c.2005G>A ENSP00000387483.2:p.Glu669Lys
ENST00000464867.1:n.424G>A