Canonical Allele Identifier: CA2383551595
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891730C= , CM000683.2:g.25891730C= GRCh38
NC_000021.8:g.27264042C= , CM000683.1:g.27264042C= GRCh37
NC_000021.7:g.26185913C= NCBI36
NG_007376.1:g.284091G=
NG_007376.2:g.284399G=

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2203G= MANE Select ENSP00000284981.4:p.Val735=
ENST00000346798.7:c.2203G= ENSP00000284981.4:p.Val735=
ENST00000348990.9:c.1978G= ENSP00000345463.5:p.Val660=
ENST00000354192.7:c.1810G= ENSP00000346129.3:p.Val604=
ENST00000357903.7:c.2146G= ENSP00000350578.3:p.Val716=
ENST00000358918.7:c.2149G= ENSP00000351796.3:p.Val717=
ENST00000359726.7:c.1873G= ENSP00000352760.4:p.Val625=
ENST00000439274.6:c.2035G= ENSP00000398879.2:p.Val679=
ENST00000440126.7:c.2131G= ENSP00000387483.2:p.Val711=
ENST00000464867.1:n.550G=
NM_000484.3:c.2203G= NP_000475.1:p.Val735=
NM_001136016.3:c.2131G= NP_001129488.1:p.Val711=
NM_001136129.2:c.1810G= NP_001129601.1:p.Val604=
NM_001136130.2:c.2035G= NP_001129602.1:p.Val679=
NM_001136131.2:c.1873G= NP_001129603.1:p.Val625=
NM_001204301.1:c.2149G= NP_001191230.1:p.Val717=
NM_001204302.1:c.2092G= NP_001191231.1:p.Val698=
NM_001204303.1:c.1924G= NP_001191232.1:p.Val642=
NM_201413.2:c.2146G= NP_958816.1:p.Val716=
NM_201414.2:c.1978G= NP_958817.1:p.Val660=
NM_000484.4:c.2203G= MANE Select NP_000475.1:p.Val735=
NM_001136129.3:c.1810G= NP_001129601.1:p.Val604=
NM_001136130.3:c.2035G= NP_001129602.1:p.Val679=
NM_001204301.2:c.2149G= NP_001191230.1:p.Val717=
NM_001204302.2:c.2092G= NP_001191231.1:p.Val698=
NM_001204303.2:c.1924G= NP_001191232.1:p.Val642=
NM_201413.3:c.2146G= NP_958816.1:p.Val716=
NM_201414.3:c.1978G= NP_958817.1:p.Val660=
NM_001136131.3:c.1873G= NP_001129603.1:p.Val625=
NM_001385253.1:c.2035G= NP_001372182.1:p.Val679=