Canonical Allele Identifier: CA409805432
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891732C>T , CM000683.2:g.25891732C>T GRCh38
NC_000021.8:g.27264044C>T , CM000683.1:g.27264044C>T GRCh37
NC_000021.7:g.26185915C>T NCBI36
NG_007376.1:g.284089G>A
NG_007376.2:g.284397G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2201G>A MANE Select ENSP00000284981.4:p.Gly734Asp
ENST00000346798.7:c.2201G>A ENSP00000284981.4:p.Gly734Asp
ENST00000348990.9:c.1976G>A ENSP00000345463.5:p.Gly659Asp
ENST00000354192.7:c.1808G>A ENSP00000346129.3:p.Gly603Asp
ENST00000357903.7:c.2144G>A ENSP00000350578.3:p.Gly715Asp
ENST00000358918.7:c.2147G>A ENSP00000351796.3:p.Gly716Asp
ENST00000359726.7:c.1871G>A ENSP00000352760.4:p.Gly624Asp
ENST00000439274.6:c.2033G>A ENSP00000398879.2:p.Gly678Asp
ENST00000440126.7:c.2129G>A ENSP00000387483.2:p.Gly710Asp
ENST00000464867.1:n.548G>A
NM_000484.3:c.2201G>A NP_000475.1:p.Gly734Asp
NM_001136016.3:c.2129G>A NP_001129488.1:p.Gly710Asp
NM_001136129.2:c.1808G>A NP_001129601.1:p.Gly603Asp
NM_001136130.2:c.2033G>A NP_001129602.1:p.Gly678Asp
NM_001136131.2:c.1871G>A NP_001129603.1:p.Gly624Asp
NM_001204301.1:c.2147G>A NP_001191230.1:p.Gly716Asp
NM_001204302.1:c.2090G>A NP_001191231.1:p.Gly697Asp
NM_001204303.1:c.1922G>A NP_001191232.1:p.Gly641Asp
NM_201413.2:c.2144G>A NP_958816.1:p.Gly715Asp
NM_201414.2:c.1976G>A NP_958817.1:p.Gly659Asp
NM_000484.4:c.2201G>A MANE Select NP_000475.1:p.Gly734Asp
NM_001136129.3:c.1808G>A NP_001129601.1:p.Gly603Asp
NM_001136130.3:c.2033G>A NP_001129602.1:p.Gly678Asp
NM_001204301.2:c.2147G>A NP_001191230.1:p.Gly716Asp
NM_001204302.2:c.2090G>A NP_001191231.1:p.Gly697Asp
NM_001204303.2:c.1922G>A NP_001191232.1:p.Gly641Asp
NM_201413.3:c.2144G>A NP_958816.1:p.Gly715Asp
NM_201414.3:c.1976G>A NP_958817.1:p.Gly659Asp
NM_001136131.3:c.1871G>A NP_001129603.1:p.Gly624Asp
NM_001385253.1:c.2033G>A NP_001372182.1:p.Gly678Asp