Canonical Allele Identifier: CA409805444
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891736G>T , CM000683.2:g.25891736G>T GRCh38
NC_000021.8:g.27264048G>T , CM000683.1:g.27264048G>T GRCh37
NC_000021.7:g.26185919G>T NCBI36
NG_007376.1:g.284085C>A
NG_007376.2:g.284393C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2197C>A MANE Select ENSP00000284981.4:p.His733Asn
ENST00000346798.7:c.2197C>A ENSP00000284981.4:p.His733Asn
ENST00000348990.9:c.1972C>A ENSP00000345463.5:p.His658Asn
ENST00000354192.7:c.1804C>A ENSP00000346129.3:p.His602Asn
ENST00000357903.7:c.2140C>A ENSP00000350578.3:p.His714Asn
ENST00000358918.7:c.2143C>A ENSP00000351796.3:p.His715Asn
ENST00000359726.7:c.1867C>A ENSP00000352760.4:p.His623Asn
ENST00000439274.6:c.2029C>A ENSP00000398879.2:p.His677Asn
ENST00000440126.7:c.2125C>A ENSP00000387483.2:p.His709Asn
ENST00000464867.1:n.544C>A
NM_000484.3:c.2197C>A NP_000475.1:p.His733Asn
NM_001136016.3:c.2125C>A NP_001129488.1:p.His709Asn
NM_001136129.2:c.1804C>A NP_001129601.1:p.His602Asn
NM_001136130.2:c.2029C>A NP_001129602.1:p.His677Asn
NM_001136131.2:c.1867C>A NP_001129603.1:p.His623Asn
NM_001204301.1:c.2143C>A NP_001191230.1:p.His715Asn
NM_001204302.1:c.2086C>A NP_001191231.1:p.His696Asn
NM_001204303.1:c.1918C>A NP_001191232.1:p.His640Asn
NM_201413.2:c.2140C>A NP_958816.1:p.His714Asn
NM_201414.2:c.1972C>A NP_958817.1:p.His658Asn
NM_000484.4:c.2197C>A MANE Select NP_000475.1:p.His733Asn
NM_001136129.3:c.1804C>A NP_001129601.1:p.His602Asn
NM_001136130.3:c.2029C>A NP_001129602.1:p.His677Asn
NM_001204301.2:c.2143C>A NP_001191230.1:p.His715Asn
NM_001204302.2:c.2086C>A NP_001191231.1:p.His696Asn
NM_001204303.2:c.1918C>A NP_001191232.1:p.His640Asn
NM_201413.3:c.2140C>A NP_958816.1:p.His714Asn
NM_201414.3:c.1972C>A NP_958817.1:p.His658Asn
NM_001136131.3:c.1867C>A NP_001129603.1:p.His623Asn
NM_001385253.1:c.2029C>A NP_001372182.1:p.His677Asn