Canonical Allele Identifier: CA409805698
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891861A>G , CM000683.2:g.25891861A>G GRCh38
NC_000021.8:g.27264173A>G , CM000683.1:g.27264173A>G GRCh37
NC_000021.7:g.26186044A>G NCBI36
NG_007376.1:g.283960T>C
NG_007376.2:g.284268T>C

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.2072T>C NP_000475.1:p.Phe691Ser
NM_001136016.3:c.2000T>C NP_001129488.1:p.Phe667Ser
NM_001136129.2:c.1679T>C NP_001129601.1:p.Phe560Ser
NM_001136130.2:c.1904T>C NP_001129602.1:p.Phe635Ser
NM_001136131.2:c.1742T>C NP_001129603.1:p.Phe581Ser
NM_001204301.1:c.2018T>C NP_001191230.1:p.Phe673Ser
NM_001204302.1:c.1961T>C NP_001191231.1:p.Phe654Ser
NM_001204303.1:c.1793T>C NP_001191232.1:p.Phe598Ser
NM_201413.2:c.2015T>C NP_958816.1:p.Phe672Ser
NM_201414.2:c.1847T>C NP_958817.1:p.Phe616Ser
NM_000484.4:c.2072T>C MANE Select NP_000475.1:p.Phe691Ser
NM_001136129.3:c.1679T>C NP_001129601.1:p.Phe560Ser
NM_001136130.3:c.1904T>C NP_001129602.1:p.Phe635Ser
NM_001204301.2:c.2018T>C NP_001191230.1:p.Phe673Ser
NM_001204302.2:c.1961T>C NP_001191231.1:p.Phe654Ser
NM_001204303.2:c.1793T>C NP_001191232.1:p.Phe598Ser
NM_201413.3:c.2015T>C NP_958816.1:p.Phe672Ser
NM_201414.3:c.1847T>C NP_958817.1:p.Phe616Ser
NM_001136131.3:c.1742T>C NP_001129603.1:p.Phe581Ser
NM_001385253.1:c.1904T>C NP_001372182.1:p.Phe635Ser
ENST00000346798.7:c.2072T>C ENSP00000284981.4:p.Phe691Ser
ENST00000348990.9:c.1847T>C ENSP00000345463.5:p.Phe616Ser
ENST00000354192.7:c.1679T>C ENSP00000346129.3:p.Phe560Ser
ENST00000357903.7:c.2015T>C ENSP00000350578.3:p.Phe672Ser
ENST00000358918.7:c.2018T>C ENSP00000351796.3:p.Phe673Ser
ENST00000359726.7:c.1742T>C ENSP00000352760.4:p.Phe581Ser
ENST00000439274.6:c.1904T>C ENSP00000398879.2:p.Phe635Ser
ENST00000440126.7:c.2000T>C ENSP00000387483.2:p.Phe667Ser
ENST00000464867.1:n.419T>C