Canonical Allele Identifier: CA2383545855
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25881358C= , CM000683.2:g.25881358C= GRCh38
NC_000021.8:g.27253669C= , CM000683.1:g.27253669C= GRCh37
NC_000021.7:g.26175540C= NCBI36
NG_007376.1:g.294464G=
NG_007376.2:g.294771G=

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2592G=
ENST00000707133.1:n.1022G=
ENST00000707134.1:n.1291G=
ENST00000346798.8:c.*312G= MANE Select ENSP00000284981.4:n.*312G=
ENST00000346798.7:c.*312G= ENSP00000284981.4:n.*312G=
ENST00000348990.9:c.*312G= ENSP00000345463.5:n.*312G=
ENST00000354192.7:c.*312G= ENSP00000346129.3:n.*312G=
ENST00000357903.7:c.*312G= ENSP00000350578.3:n.*312G=
ENST00000359726.7:c.*312G= ENSP00000352760.4:n.*312G=
ENST00000439274.6:c.*312G= ENSP00000398879.2:n.*312G=
ENST00000440126.7:c.*312G= ENSP00000387483.2:n.*312G=
NM_000484.3:c.*312G= NP_000475.1:n.*312G=
NM_001136016.3:c.*312G= NP_001129488.1:n.*312G=
NM_001136129.2:c.*312G= NP_001129601.1:n.*312G=
NM_001136130.2:c.*312G= NP_001129602.1:n.*312G=
NM_001136131.2:c.*312G= NP_001129603.1:n.*312G=
NM_001204301.1:c.*312G= NP_001191230.1:n.*312G=
NM_001204302.1:c.*312G= NP_001191231.1:n.*312G=
NM_001204303.1:c.*312G= NP_001191232.1:n.*312G=
NM_201413.2:c.*312G= NP_958816.1:n.*312G=
NM_201414.2:c.*312G= NP_958817.1:n.*312G=
NM_000484.4:c.*312G= MANE Select NP_000475.1:n.*312G=
NM_001136129.3:c.*312G= NP_001129601.1:n.*312G=
NM_001136130.3:c.*312G= NP_001129602.1:n.*312G=
NM_001204301.2:c.*312G= NP_001191230.1:n.*312G=
NM_001204302.2:c.*312G= NP_001191231.1:n.*312G=
NM_001204303.2:c.*312G= NP_001191232.1:n.*312G=
NM_201413.3:c.*312G= NP_958816.1:n.*312G=
NM_201414.3:c.*312G= NP_958817.1:n.*312G=
NM_001136131.3:c.*312G= NP_001129603.1:n.*312G=
NM_001385253.1:c.*312G= NP_001372182.1:n.*312G=