Canonical Allele Identifier: CA409806552
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897652T>G , CM000683.2:g.25897652T>G GRCh38
NC_000021.8:g.27269964T>G , CM000683.1:g.27269964T>G GRCh37
NC_000021.7:g.26191835T>G NCBI36
NG_007376.1:g.278169A>C
NG_007376.2:g.278477A>C

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.1985A>C NP_000475.1:p.Lys662Thr
NM_001136016.3:c.1913A>C NP_001129488.1:p.Lys638Thr
NM_001136129.2:c.1592A>C NP_001129601.1:p.Lys531Thr
NM_001136130.2:c.1817A>C NP_001129602.1:p.Lys606Thr
NM_001136131.2:c.1655A>C NP_001129603.1:p.Lys552Thr
NM_001204301.1:c.1931A>C NP_001191230.1:p.Lys644Thr
NM_001204302.1:c.1874A>C NP_001191231.1:p.Lys625Thr
NM_001204303.1:c.1706A>C NP_001191232.1:p.Lys569Thr
NM_201413.2:c.1928A>C NP_958816.1:p.Lys643Thr
NM_201414.2:c.1760A>C NP_958817.1:p.Lys587Thr
NM_000484.4:c.1985A>C MANE Select NP_000475.1:p.Lys662Thr
NM_001136129.3:c.1592A>C NP_001129601.1:p.Lys531Thr
NM_001136130.3:c.1817A>C NP_001129602.1:p.Lys606Thr
NM_001204301.2:c.1931A>C NP_001191230.1:p.Lys644Thr
NM_001204302.2:c.1874A>C NP_001191231.1:p.Lys625Thr
NM_001204303.2:c.1706A>C NP_001191232.1:p.Lys569Thr
NM_201413.3:c.1928A>C NP_958816.1:p.Lys643Thr
NM_201414.3:c.1760A>C NP_958817.1:p.Lys587Thr
NM_001136131.3:c.1655A>C NP_001129603.1:p.Lys552Thr
NM_001385253.1:c.1817A>C NP_001372182.1:p.Lys606Thr
ENST00000346798.7:c.1985A>C ENSP00000284981.4:p.Lys662Thr
ENST00000348990.9:c.1760A>C ENSP00000345463.5:p.Lys587Thr
ENST00000354192.7:c.1592A>C ENSP00000346129.3:p.Lys531Thr
ENST00000357903.7:c.1928A>C ENSP00000350578.3:p.Lys643Thr
ENST00000358918.7:c.1931A>C ENSP00000351796.3:p.Lys644Thr
ENST00000359726.7:c.1655A>C ENSP00000352760.4:p.Lys552Thr
ENST00000439274.6:c.1817A>C ENSP00000398879.2:p.Lys606Thr
ENST00000440126.7:c.1913A>C ENSP00000387483.2:p.Lys638Thr
ENST00000464867.1:n.332A>C