Canonical Allele Identifier: CA409805551
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891783A>T , CM000683.2:g.25891783A>T GRCh38
NC_000021.8:g.27264095A>T , CM000683.1:g.27264095A>T GRCh37
NC_000021.7:g.26185966A>T NCBI36
NG_007376.1:g.284038T>A
NG_007376.2:g.284346T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2150T>A MANE Select ENSP00000284981.4:p.Val717Asp
ENST00000346798.7:c.2150T>A ENSP00000284981.4:p.Val717Asp
ENST00000348990.9:c.1925T>A ENSP00000345463.5:p.Val642Asp
ENST00000354192.7:c.1757T>A ENSP00000346129.3:p.Val586Asp
ENST00000357903.7:c.2093T>A ENSP00000350578.3:p.Val698Asp
ENST00000358918.7:c.2096T>A ENSP00000351796.3:p.Val699Asp
ENST00000359726.7:c.1820T>A ENSP00000352760.4:p.Val607Asp
ENST00000439274.6:c.1982T>A ENSP00000398879.2:p.Val661Asp
ENST00000440126.7:c.2078T>A ENSP00000387483.2:p.Val693Asp
ENST00000464867.1:n.497T>A
NM_000484.3:c.2150T>A NP_000475.1:p.Val717Asp
NM_001136016.3:c.2078T>A NP_001129488.1:p.Val693Asp
NM_001136129.2:c.1757T>A NP_001129601.1:p.Val586Asp
NM_001136130.2:c.1982T>A NP_001129602.1:p.Val661Asp
NM_001136131.2:c.1820T>A NP_001129603.1:p.Val607Asp
NM_001204301.1:c.2096T>A NP_001191230.1:p.Val699Asp
NM_001204302.1:c.2039T>A NP_001191231.1:p.Val680Asp
NM_001204303.1:c.1871T>A NP_001191232.1:p.Val624Asp
NM_201413.2:c.2093T>A NP_958816.1:p.Val698Asp
NM_201414.2:c.1925T>A NP_958817.1:p.Val642Asp
NM_000484.4:c.2150T>A MANE Select NP_000475.1:p.Val717Asp
NM_001136129.3:c.1757T>A NP_001129601.1:p.Val586Asp
NM_001136130.3:c.1982T>A NP_001129602.1:p.Val661Asp
NM_001204301.2:c.2096T>A NP_001191230.1:p.Val699Asp
NM_001204302.2:c.2039T>A NP_001191231.1:p.Val680Asp
NM_001204303.2:c.1871T>A NP_001191232.1:p.Val624Asp
NM_201413.3:c.2093T>A NP_958816.1:p.Val698Asp
NM_201414.3:c.1925T>A NP_958817.1:p.Val642Asp
NM_001136131.3:c.1820T>A NP_001129603.1:p.Val607Asp
NM_001385253.1:c.1982T>A NP_001372182.1:p.Val661Asp