Canonical Allele Identifier: CA409805443
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2197C>T MANE Select ENSP00000284981.4:p.His733Tyr
ENST00000346798.7:c.2197C>T ENSP00000284981.4:p.His733Tyr
ENST00000348990.9:c.1972C>T ENSP00000345463.5:p.His658Tyr
ENST00000354192.7:c.1804C>T ENSP00000346129.3:p.His602Tyr
ENST00000357903.7:c.2140C>T ENSP00000350578.3:p.His714Tyr
ENST00000358918.7:c.2143C>T ENSP00000351796.3:p.His715Tyr
ENST00000359726.7:c.1867C>T ENSP00000352760.4:p.His623Tyr
ENST00000439274.6:c.2029C>T ENSP00000398879.2:p.His677Tyr
ENST00000440126.7:c.2125C>T ENSP00000387483.2:p.His709Tyr
ENST00000464867.1:n.544C>T
NM_000484.3:c.2197C>T NP_000475.1:p.His733Tyr
NM_001136016.3:c.2125C>T NP_001129488.1:p.His709Tyr
NM_001136129.2:c.1804C>T NP_001129601.1:p.His602Tyr
NM_001136130.2:c.2029C>T NP_001129602.1:p.His677Tyr
NM_001136131.2:c.1867C>T NP_001129603.1:p.His623Tyr
NM_001204301.1:c.2143C>T NP_001191230.1:p.His715Tyr
NM_001204302.1:c.2086C>T NP_001191231.1:p.His696Tyr
NM_001204303.1:c.1918C>T NP_001191232.1:p.His640Tyr
NM_201413.2:c.2140C>T NP_958816.1:p.His714Tyr
NM_201414.2:c.1972C>T NP_958817.1:p.His658Tyr
NM_000484.4:c.2197C>T MANE Select NP_000475.1:p.His733Tyr
NM_001136129.3:c.1804C>T NP_001129601.1:p.His602Tyr
NM_001136130.3:c.2029C>T NP_001129602.1:p.His677Tyr
NM_001204301.2:c.2143C>T NP_001191230.1:p.His715Tyr
NM_001204302.2:c.2086C>T NP_001191231.1:p.His696Tyr
NM_001204303.2:c.1918C>T NP_001191232.1:p.His640Tyr
NM_201413.3:c.2140C>T NP_958816.1:p.His714Tyr
NM_201414.3:c.1972C>T NP_958817.1:p.His658Tyr
NM_001136131.3:c.1867C>T NP_001129603.1:p.His623Tyr
NM_001385253.1:c.2029C>T NP_001372182.1:p.His677Tyr