Canonical Allele Identifier: CA409806542
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897649G>C , CM000683.2:g.25897649G>C GRCh38
NC_000021.8:g.27269961G>C , CM000683.1:g.27269961G>C GRCh37
NC_000021.7:g.26191832G>C NCBI36
NG_007376.1:g.278172C>G
NG_007376.2:g.278480C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.1988C>G MANE Select ENSP00000284981.4:p.Thr663Arg
ENST00000346798.7:c.1988C>G ENSP00000284981.4:p.Thr663Arg
ENST00000348990.9:c.1763C>G ENSP00000345463.5:p.Thr588Arg
ENST00000354192.7:c.1595C>G ENSP00000346129.3:p.Thr532Arg
ENST00000357903.7:c.1931C>G ENSP00000350578.3:p.Thr644Arg
ENST00000358918.7:c.1934C>G ENSP00000351796.3:p.Thr645Arg
ENST00000359726.7:c.1658C>G ENSP00000352760.4:p.Thr553Arg
ENST00000439274.6:c.1820C>G ENSP00000398879.2:p.Thr607Arg
ENST00000440126.7:c.1916C>G ENSP00000387483.2:p.Thr639Arg
ENST00000464867.1:n.335C>G
NM_000484.3:c.1988C>G NP_000475.1:p.Thr663Arg
NM_001136016.3:c.1916C>G NP_001129488.1:p.Thr639Arg
NM_001136129.2:c.1595C>G NP_001129601.1:p.Thr532Arg
NM_001136130.2:c.1820C>G NP_001129602.1:p.Thr607Arg
NM_001136131.2:c.1658C>G NP_001129603.1:p.Thr553Arg
NM_001204301.1:c.1934C>G NP_001191230.1:p.Thr645Arg
NM_001204302.1:c.1877C>G NP_001191231.1:p.Thr626Arg
NM_001204303.1:c.1709C>G NP_001191232.1:p.Thr570Arg
NM_201413.2:c.1931C>G NP_958816.1:p.Thr644Arg
NM_201414.2:c.1763C>G NP_958817.1:p.Thr588Arg
NM_000484.4:c.1988C>G MANE Select NP_000475.1:p.Thr663Arg
NM_001136129.3:c.1595C>G NP_001129601.1:p.Thr532Arg
NM_001136130.3:c.1820C>G NP_001129602.1:p.Thr607Arg
NM_001204301.2:c.1934C>G NP_001191230.1:p.Thr645Arg
NM_001204302.2:c.1877C>G NP_001191231.1:p.Thr626Arg
NM_001204303.2:c.1709C>G NP_001191232.1:p.Thr570Arg
NM_201413.3:c.1931C>G NP_958816.1:p.Thr644Arg
NM_201414.3:c.1763C>G NP_958817.1:p.Thr588Arg
NM_001136131.3:c.1658C>G NP_001129603.1:p.Thr553Arg
NM_001385253.1:c.1820C>G NP_001372182.1:p.Thr607Arg