Canonical Allele Identifier: CA409806368
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897608G>C , CM000683.2:g.25897608G>C GRCh38
NC_000021.8:g.27269920G>C , CM000683.1:g.27269920G>C GRCh37
NC_000021.7:g.26191791G>C NCBI36
NG_007376.1:g.278213C>G
NG_007376.2:g.278521C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.1996C>G
ENST00000707133.1:n.426C>G
ENST00000707134.1:n.695C>G
ENST00000346798.8:c.2029C>G MANE Select ENSP00000284981.4:p.His677Asp
ENST00000346798.7:c.2029C>G ENSP00000284981.4:p.His677Asp
ENST00000348990.9:c.1804C>G ENSP00000345463.5:p.His602Asp
ENST00000354192.7:c.1636C>G ENSP00000346129.3:p.His546Asp
ENST00000357903.7:c.1972C>G ENSP00000350578.3:p.His658Asp
ENST00000358918.7:c.1975C>G ENSP00000351796.3:p.His659Asp
ENST00000359726.7:c.1699C>G ENSP00000352760.4:p.His567Asp
ENST00000439274.6:c.1861C>G ENSP00000398879.2:p.His621Asp
ENST00000440126.7:c.1957C>G ENSP00000387483.2:p.His653Asp
ENST00000464867.1:n.376C>G
NM_000484.3:c.2029C>G NP_000475.1:p.His677Asp
NM_001136016.3:c.1957C>G NP_001129488.1:p.His653Asp
NM_001136129.2:c.1636C>G NP_001129601.1:p.His546Asp
NM_001136130.2:c.1861C>G NP_001129602.1:p.His621Asp
NM_001136131.2:c.1699C>G NP_001129603.1:p.His567Asp
NM_001204301.1:c.1975C>G NP_001191230.1:p.His659Asp
NM_001204302.1:c.1918C>G NP_001191231.1:p.His640Asp
NM_001204303.1:c.1750C>G NP_001191232.1:p.His584Asp
NM_201413.2:c.1972C>G NP_958816.1:p.His658Asp
NM_201414.2:c.1804C>G NP_958817.1:p.His602Asp
NM_000484.4:c.2029C>G MANE Select NP_000475.1:p.His677Asp
NM_001136129.3:c.1636C>G NP_001129601.1:p.His546Asp
NM_001136130.3:c.1861C>G NP_001129602.1:p.His621Asp
NM_001204301.2:c.1975C>G NP_001191230.1:p.His659Asp
NM_001204302.2:c.1918C>G NP_001191231.1:p.His640Asp
NM_001204303.2:c.1750C>G NP_001191232.1:p.His584Asp
NM_201413.3:c.1972C>G NP_958816.1:p.His658Asp
NM_201414.3:c.1804C>G NP_958817.1:p.His602Asp
NM_001136131.3:c.1699C>G NP_001129603.1:p.His567Asp
NM_001385253.1:c.1861C>G NP_001372182.1:p.His621Asp