Canonical Allele Identifier: CA2383554930
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897628T= , CM000683.2:g.25897628T= GRCh38
NC_000021.8:g.27269940T= , CM000683.1:g.27269940T= GRCh37
NC_000021.7:g.26191811T= NCBI36
NG_007376.1:g.278193A=
NG_007376.2:g.278501A=

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1976A=
ENST00000707133.1:n.406A=
ENST00000707134.1:n.675A=
ENST00000346798.8:c.2009A= MANE Select ENSP00000284981.4:p.Lys670=
ENST00000346798.7:c.2009A= ENSP00000284981.4:p.Lys670=
ENST00000348990.9:c.1784A= ENSP00000345463.5:p.Lys595=
ENST00000354192.7:c.1616A= ENSP00000346129.3:p.Lys539=
ENST00000357903.7:c.1952A= ENSP00000350578.3:p.Lys651=
ENST00000358918.7:c.1955A= ENSP00000351796.3:p.Lys652=
ENST00000359726.7:c.1679A= ENSP00000352760.4:p.Lys560=
ENST00000439274.6:c.1841A= ENSP00000398879.2:p.Lys614=
ENST00000440126.7:c.1937A= ENSP00000387483.2:p.Lys646=
ENST00000464867.1:n.356A=
NM_000484.3:c.2009A= NP_000475.1:p.Lys670=
NM_001136016.3:c.1937A= NP_001129488.1:p.Lys646=
NM_001136129.2:c.1616A= NP_001129601.1:p.Lys539=
NM_001136130.2:c.1841A= NP_001129602.1:p.Lys614=
NM_001136131.2:c.1679A= NP_001129603.1:p.Lys560=
NM_001204301.1:c.1955A= NP_001191230.1:p.Lys652=
NM_001204302.1:c.1898A= NP_001191231.1:p.Lys633=
NM_001204303.1:c.1730A= NP_001191232.1:p.Lys577=
NM_201413.2:c.1952A= NP_958816.1:p.Lys651=
NM_201414.2:c.1784A= NP_958817.1:p.Lys595=
NM_000484.4:c.2009A= MANE Select NP_000475.1:p.Lys670=
NM_001136129.3:c.1616A= NP_001129601.1:p.Lys539=
NM_001136130.3:c.1841A= NP_001129602.1:p.Lys614=
NM_001204301.2:c.1955A= NP_001191230.1:p.Lys652=
NM_001204302.2:c.1898A= NP_001191231.1:p.Lys633=
NM_001204303.2:c.1730A= NP_001191232.1:p.Lys577=
NM_201413.3:c.1952A= NP_958816.1:p.Lys651=
NM_201414.3:c.1784A= NP_958817.1:p.Lys595=
NM_001136131.3:c.1679A= NP_001129603.1:p.Lys560=
NM_001385253.1:c.1841A= NP_001372182.1:p.Lys614=