Canonical Allele Identifier: CA409805452
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891739G>T , CM000683.2:g.25891739G>T GRCh38
NC_000021.8:g.27264051G>T , CM000683.1:g.27264051G>T GRCh37
NC_000021.7:g.26185922G>T NCBI36
NG_007376.1:g.284082C>A
NG_007376.2:g.284390C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2194C>A MANE Select ENSP00000284981.4:p.His732Asn
ENST00000346798.7:c.2194C>A ENSP00000284981.4:p.His732Asn
ENST00000348990.9:c.1969C>A ENSP00000345463.5:p.His657Asn
ENST00000354192.7:c.1801C>A ENSP00000346129.3:p.His601Asn
ENST00000357903.7:c.2137C>A ENSP00000350578.3:p.His713Asn
ENST00000358918.7:c.2140C>A ENSP00000351796.3:p.His714Asn
ENST00000359726.7:c.1864C>A ENSP00000352760.4:p.His622Asn
ENST00000439274.6:c.2026C>A ENSP00000398879.2:p.His676Asn
ENST00000440126.7:c.2122C>A ENSP00000387483.2:p.His708Asn
ENST00000464867.1:n.541C>A
NM_000484.3:c.2194C>A NP_000475.1:p.His732Asn
NM_001136016.3:c.2122C>A NP_001129488.1:p.His708Asn
NM_001136129.2:c.1801C>A NP_001129601.1:p.His601Asn
NM_001136130.2:c.2026C>A NP_001129602.1:p.His676Asn
NM_001136131.2:c.1864C>A NP_001129603.1:p.His622Asn
NM_001204301.1:c.2140C>A NP_001191230.1:p.His714Asn
NM_001204302.1:c.2083C>A NP_001191231.1:p.His695Asn
NM_001204303.1:c.1915C>A NP_001191232.1:p.His639Asn
NM_201413.2:c.2137C>A NP_958816.1:p.His713Asn
NM_201414.2:c.1969C>A NP_958817.1:p.His657Asn
NM_000484.4:c.2194C>A MANE Select NP_000475.1:p.His732Asn
NM_001136129.3:c.1801C>A NP_001129601.1:p.His601Asn
NM_001136130.3:c.2026C>A NP_001129602.1:p.His676Asn
NM_001204301.2:c.2140C>A NP_001191230.1:p.His714Asn
NM_001204302.2:c.2083C>A NP_001191231.1:p.His695Asn
NM_001204303.2:c.1915C>A NP_001191232.1:p.His639Asn
NM_201413.3:c.2137C>A NP_958816.1:p.His713Asn
NM_201414.3:c.1969C>A NP_958817.1:p.His657Asn
NM_001136131.3:c.1864C>A NP_001129603.1:p.His622Asn
NM_001385253.1:c.2026C>A NP_001372182.1:p.His676Asn