Canonical Allele Identifier: CA409805692
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891859C>A , CM000683.2:g.25891859C>A GRCh38
NC_000021.8:g.27264171C>A , CM000683.1:g.27264171C>A GRCh37
NC_000021.7:g.26186042C>A NCBI36
NG_007376.1:g.283962G>T
NG_007376.2:g.284270G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2074G>T MANE Select ENSP00000284981.4:p.Ala692Ser
ENST00000346798.7:c.2074G>T ENSP00000284981.4:p.Ala692Ser
ENST00000348990.9:c.1849G>T ENSP00000345463.5:p.Ala617Ser
ENST00000354192.7:c.1681G>T ENSP00000346129.3:p.Ala561Ser
ENST00000357903.7:c.2017G>T ENSP00000350578.3:p.Ala673Ser
ENST00000358918.7:c.2020G>T ENSP00000351796.3:p.Ala674Ser
ENST00000359726.7:c.1744G>T ENSP00000352760.4:p.Ala582Ser
ENST00000439274.6:c.1906G>T ENSP00000398879.2:p.Ala636Ser
ENST00000440126.7:c.2002G>T ENSP00000387483.2:p.Ala668Ser
ENST00000464867.1:n.421G>T
NM_000484.3:c.2074G>T NP_000475.1:p.Ala692Ser
NM_001136016.3:c.2002G>T NP_001129488.1:p.Ala668Ser
NM_001136129.2:c.1681G>T NP_001129601.1:p.Ala561Ser
NM_001136130.2:c.1906G>T NP_001129602.1:p.Ala636Ser
NM_001136131.2:c.1744G>T NP_001129603.1:p.Ala582Ser
NM_001204301.1:c.2020G>T NP_001191230.1:p.Ala674Ser
NM_001204302.1:c.1963G>T NP_001191231.1:p.Ala655Ser
NM_001204303.1:c.1795G>T NP_001191232.1:p.Ala599Ser
NM_201413.2:c.2017G>T NP_958816.1:p.Ala673Ser
NM_201414.2:c.1849G>T NP_958817.1:p.Ala617Ser
NM_000484.4:c.2074G>T MANE Select NP_000475.1:p.Ala692Ser
NM_001136129.3:c.1681G>T NP_001129601.1:p.Ala561Ser
NM_001136130.3:c.1906G>T NP_001129602.1:p.Ala636Ser
NM_001204301.2:c.2020G>T NP_001191230.1:p.Ala674Ser
NM_001204302.2:c.1963G>T NP_001191231.1:p.Ala655Ser
NM_001204303.2:c.1795G>T NP_001191232.1:p.Ala599Ser
NM_201413.3:c.2017G>T NP_958816.1:p.Ala673Ser
NM_201414.3:c.1849G>T NP_958817.1:p.Ala617Ser
NM_001136131.3:c.1744G>T NP_001129603.1:p.Ala582Ser
NM_001385253.1:c.1906G>T NP_001372182.1:p.Ala636Ser