Canonical Allele Identifier: CA409805436
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891733C>T , CM000683.2:g.25891733C>T GRCh38
NC_000021.8:g.27264045C>T , CM000683.1:g.27264045C>T GRCh37
NC_000021.7:g.26185916C>T NCBI36
NG_007376.1:g.284088G>A
NG_007376.2:g.284396G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2200G>A MANE Select ENSP00000284981.4:p.Gly734Ser
ENST00000346798.7:c.2200G>A ENSP00000284981.4:p.Gly734Ser
ENST00000348990.9:c.1975G>A ENSP00000345463.5:p.Gly659Ser
ENST00000354192.7:c.1807G>A ENSP00000346129.3:p.Gly603Ser
ENST00000357903.7:c.2143G>A ENSP00000350578.3:p.Gly715Ser
ENST00000358918.7:c.2146G>A ENSP00000351796.3:p.Gly716Ser
ENST00000359726.7:c.1870G>A ENSP00000352760.4:p.Gly624Ser
ENST00000439274.6:c.2032G>A ENSP00000398879.2:p.Gly678Ser
ENST00000440126.7:c.2128G>A ENSP00000387483.2:p.Gly710Ser
ENST00000464867.1:n.547G>A
NM_000484.3:c.2200G>A NP_000475.1:p.Gly734Ser
NM_001136016.3:c.2128G>A NP_001129488.1:p.Gly710Ser
NM_001136129.2:c.1807G>A NP_001129601.1:p.Gly603Ser
NM_001136130.2:c.2032G>A NP_001129602.1:p.Gly678Ser
NM_001136131.2:c.1870G>A NP_001129603.1:p.Gly624Ser
NM_001204301.1:c.2146G>A NP_001191230.1:p.Gly716Ser
NM_001204302.1:c.2089G>A NP_001191231.1:p.Gly697Ser
NM_001204303.1:c.1921G>A NP_001191232.1:p.Gly641Ser
NM_201413.2:c.2143G>A NP_958816.1:p.Gly715Ser
NM_201414.2:c.1975G>A NP_958817.1:p.Gly659Ser
NM_000484.4:c.2200G>A MANE Select NP_000475.1:p.Gly734Ser
NM_001136129.3:c.1807G>A NP_001129601.1:p.Gly603Ser
NM_001136130.3:c.2032G>A NP_001129602.1:p.Gly678Ser
NM_001204301.2:c.2146G>A NP_001191230.1:p.Gly716Ser
NM_001204302.2:c.2089G>A NP_001191231.1:p.Gly697Ser
NM_001204303.2:c.1921G>A NP_001191232.1:p.Gly641Ser
NM_201413.3:c.2143G>A NP_958816.1:p.Gly715Ser
NM_201414.3:c.1975G>A NP_958817.1:p.Gly659Ser
NM_001136131.3:c.1870G>A NP_001129603.1:p.Gly624Ser
NM_001385253.1:c.2032G>A NP_001372182.1:p.Gly678Ser