Canonical Allele Identifier: CA409806571
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897662T>A , CM000683.2:g.25897662T>A GRCh38
NC_000021.8:g.27269974T>A , CM000683.1:g.27269974T>A GRCh37
NC_000021.7:g.26191845T>A NCBI36
NG_007376.1:g.278159A>T
NG_007376.2:g.278467A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1942A>T
ENST00000707133.1:n.372A>T
ENST00000707134.1:n.641A>T
ENST00000346798.8:c.1975A>T MANE Select ENSP00000284981.4:p.Thr659Ser
ENST00000346798.7:c.1975A>T ENSP00000284981.4:p.Thr659Ser
ENST00000348990.9:c.1750A>T ENSP00000345463.5:p.Thr584Ser
ENST00000354192.7:c.1582A>T ENSP00000346129.3:p.Thr528Ser
ENST00000357903.7:c.1918A>T ENSP00000350578.3:p.Thr640Ser
ENST00000358918.7:c.1921A>T ENSP00000351796.3:p.Thr641Ser
ENST00000359726.7:c.1645A>T ENSP00000352760.4:p.Thr549Ser
ENST00000439274.6:c.1807A>T ENSP00000398879.2:p.Thr603Ser
ENST00000440126.7:c.1903A>T ENSP00000387483.2:p.Thr635Ser
ENST00000464867.1:n.322A>T
NM_000484.3:c.1975A>T NP_000475.1:p.Thr659Ser
NM_001136016.3:c.1903A>T NP_001129488.1:p.Thr635Ser
NM_001136129.2:c.1582A>T NP_001129601.1:p.Thr528Ser
NM_001136130.2:c.1807A>T NP_001129602.1:p.Thr603Ser
NM_001136131.2:c.1645A>T NP_001129603.1:p.Thr549Ser
NM_001204301.1:c.1921A>T NP_001191230.1:p.Thr641Ser
NM_001204302.1:c.1864A>T NP_001191231.1:p.Thr622Ser
NM_001204303.1:c.1696A>T NP_001191232.1:p.Thr566Ser
NM_201413.2:c.1918A>T NP_958816.1:p.Thr640Ser
NM_201414.2:c.1750A>T NP_958817.1:p.Thr584Ser
NM_000484.4:c.1975A>T MANE Select NP_000475.1:p.Thr659Ser
NM_001136129.3:c.1582A>T NP_001129601.1:p.Thr528Ser
NM_001136130.3:c.1807A>T NP_001129602.1:p.Thr603Ser
NM_001204301.2:c.1921A>T NP_001191230.1:p.Thr641Ser
NM_001204302.2:c.1864A>T NP_001191231.1:p.Thr622Ser
NM_001204303.2:c.1696A>T NP_001191232.1:p.Thr566Ser
NM_201413.3:c.1918A>T NP_958816.1:p.Thr640Ser
NM_201414.3:c.1750A>T NP_958817.1:p.Thr584Ser
NM_001136131.3:c.1645A>T NP_001129603.1:p.Thr549Ser
NM_001385253.1:c.1807A>T NP_001372182.1:p.Thr603Ser