Canonical Allele Identifier: CA409806570
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs1423507031

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897661G>T , CM000683.2:g.25897661G>T GRCh38
NC_000021.8:g.27269973G>T , CM000683.1:g.27269973G>T GRCh37
NC_000021.7:g.26191844G>T NCBI36
NG_007376.1:g.278160C>A
NG_007376.2:g.278468C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1943C>A
ENST00000707133.1:n.373C>A
ENST00000707134.1:n.642C>A
ENST00000346798.8:c.1976C>A MANE Select ENSP00000284981.4:p.Thr659Lys
ENST00000346798.7:c.1976C>A ENSP00000284981.4:p.Thr659Lys
ENST00000348990.9:c.1751C>A ENSP00000345463.5:p.Thr584Lys
ENST00000354192.7:c.1583C>A ENSP00000346129.3:p.Thr528Lys
ENST00000357903.7:c.1919C>A ENSP00000350578.3:p.Thr640Lys
ENST00000358918.7:c.1922C>A ENSP00000351796.3:p.Thr641Lys
ENST00000359726.7:c.1646C>A ENSP00000352760.4:p.Thr549Lys
ENST00000439274.6:c.1808C>A ENSP00000398879.2:p.Thr603Lys
ENST00000440126.7:c.1904C>A ENSP00000387483.2:p.Thr635Lys
ENST00000464867.1:n.323C>A
NM_000484.3:c.1976C>A NP_000475.1:p.Thr659Lys
NM_001136016.3:c.1904C>A NP_001129488.1:p.Thr635Lys
NM_001136129.2:c.1583C>A NP_001129601.1:p.Thr528Lys
NM_001136130.2:c.1808C>A NP_001129602.1:p.Thr603Lys
NM_001136131.2:c.1646C>A NP_001129603.1:p.Thr549Lys
NM_001204301.1:c.1922C>A NP_001191230.1:p.Thr641Lys
NM_001204302.1:c.1865C>A NP_001191231.1:p.Thr622Lys
NM_001204303.1:c.1697C>A NP_001191232.1:p.Thr566Lys
NM_201413.2:c.1919C>A NP_958816.1:p.Thr640Lys
NM_201414.2:c.1751C>A NP_958817.1:p.Thr584Lys
NM_000484.4:c.1976C>A MANE Select NP_000475.1:p.Thr659Lys
NM_001136129.3:c.1583C>A NP_001129601.1:p.Thr528Lys
NM_001136130.3:c.1808C>A NP_001129602.1:p.Thr603Lys
NM_001204301.2:c.1922C>A NP_001191230.1:p.Thr641Lys
NM_001204302.2:c.1865C>A NP_001191231.1:p.Thr622Lys
NM_001204303.2:c.1697C>A NP_001191232.1:p.Thr566Lys
NM_201413.3:c.1919C>A NP_958816.1:p.Thr640Lys
NM_201414.3:c.1751C>A NP_958817.1:p.Thr584Lys
NM_001136131.3:c.1646C>A NP_001129603.1:p.Thr549Lys
NM_001385253.1:c.1808C>A NP_001372182.1:p.Thr603Lys