Canonical Allele Identifier: CA409805460
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891744G>A , CM000683.2:g.25891744G>A GRCh38
NC_000021.8:g.27264056G>A , CM000683.1:g.27264056G>A GRCh37
NC_000021.7:g.26185927G>A NCBI36
NG_007376.1:g.284077C>T
NG_007376.2:g.284385C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2156C>T
ENST00000707133.1:n.586C>T
ENST00000707134.1:n.855C>T
ENST00000346798.8:c.2189C>T MANE Select ENSP00000284981.4:p.Ser730Phe
ENST00000346798.7:c.2189C>T ENSP00000284981.4:p.Ser730Phe
ENST00000348990.9:c.1964C>T ENSP00000345463.5:p.Ser655Phe
ENST00000354192.7:c.1796C>T ENSP00000346129.3:p.Ser599Phe
ENST00000357903.7:c.2132C>T ENSP00000350578.3:p.Ser711Phe
ENST00000358918.7:c.2135C>T ENSP00000351796.3:p.Ser712Phe
ENST00000359726.7:c.1859C>T ENSP00000352760.4:p.Ser620Phe
ENST00000439274.6:c.2021C>T ENSP00000398879.2:p.Ser674Phe
ENST00000440126.7:c.2117C>T ENSP00000387483.2:p.Ser706Phe
ENST00000464867.1:n.536C>T
NM_000484.3:c.2189C>T NP_000475.1:p.Ser730Phe
NM_001136016.3:c.2117C>T NP_001129488.1:p.Ser706Phe
NM_001136129.2:c.1796C>T NP_001129601.1:p.Ser599Phe
NM_001136130.2:c.2021C>T NP_001129602.1:p.Ser674Phe
NM_001136131.2:c.1859C>T NP_001129603.1:p.Ser620Phe
NM_001204301.1:c.2135C>T NP_001191230.1:p.Ser712Phe
NM_001204302.1:c.2078C>T NP_001191231.1:p.Ser693Phe
NM_001204303.1:c.1910C>T NP_001191232.1:p.Ser637Phe
NM_201413.2:c.2132C>T NP_958816.1:p.Ser711Phe
NM_201414.2:c.1964C>T NP_958817.1:p.Ser655Phe
NM_000484.4:c.2189C>T MANE Select NP_000475.1:p.Ser730Phe
NM_001136129.3:c.1796C>T NP_001129601.1:p.Ser599Phe
NM_001136130.3:c.2021C>T NP_001129602.1:p.Ser674Phe
NM_001204301.2:c.2135C>T NP_001191230.1:p.Ser712Phe
NM_001204302.2:c.2078C>T NP_001191231.1:p.Ser693Phe
NM_001204303.2:c.1910C>T NP_001191232.1:p.Ser637Phe
NM_201413.3:c.2132C>T NP_958816.1:p.Ser711Phe
NM_201414.3:c.1964C>T NP_958817.1:p.Ser655Phe
NM_001136131.3:c.1859C>T NP_001129603.1:p.Ser620Phe
NM_001385253.1:c.2021C>T NP_001372182.1:p.Ser674Phe