Canonical Allele Identifier: CA409805420
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891726A>G , CM000683.2:g.25891726A>G GRCh38
NC_000021.8:g.27264038A>G , CM000683.1:g.27264038A>G GRCh37
NC_000021.7:g.26185909A>G NCBI36
NG_007376.1:g.284095T>C
NG_007376.2:g.284403T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2207T>C MANE Select ENSP00000284981.4:p.Val736Ala
ENST00000346798.7:c.2207T>C ENSP00000284981.4:p.Val736Ala
ENST00000348990.9:c.1982T>C ENSP00000345463.5:p.Val661Ala
ENST00000354192.7:c.1814T>C ENSP00000346129.3:p.Val605Ala
ENST00000357903.7:c.2150T>C ENSP00000350578.3:p.Val717Ala
ENST00000358918.7:c.2153T>C ENSP00000351796.3:p.Val718Ala
ENST00000359726.7:c.1877T>C ENSP00000352760.4:p.Val626Ala
ENST00000439274.6:c.2039T>C ENSP00000398879.2:p.Val680Ala
ENST00000440126.7:c.2135T>C ENSP00000387483.2:p.Val712Ala
ENST00000464867.1:n.554T>C
NM_000484.3:c.2207T>C NP_000475.1:p.Val736Ala
NM_001136016.3:c.2135T>C NP_001129488.1:p.Val712Ala
NM_001136129.2:c.1814T>C NP_001129601.1:p.Val605Ala
NM_001136130.2:c.2039T>C NP_001129602.1:p.Val680Ala
NM_001136131.2:c.1877T>C NP_001129603.1:p.Val626Ala
NM_001204301.1:c.2153T>C NP_001191230.1:p.Val718Ala
NM_001204302.1:c.2096T>C NP_001191231.1:p.Val699Ala
NM_001204303.1:c.1928T>C NP_001191232.1:p.Val643Ala
NM_201413.2:c.2150T>C NP_958816.1:p.Val717Ala
NM_201414.2:c.1982T>C NP_958817.1:p.Val661Ala
NM_000484.4:c.2207T>C MANE Select NP_000475.1:p.Val736Ala
NM_001136129.3:c.1814T>C NP_001129601.1:p.Val605Ala
NM_001136130.3:c.2039T>C NP_001129602.1:p.Val680Ala
NM_001204301.2:c.2153T>C NP_001191230.1:p.Val718Ala
NM_001204302.2:c.2096T>C NP_001191231.1:p.Val699Ala
NM_001204303.2:c.1928T>C NP_001191232.1:p.Val643Ala
NM_201413.3:c.2150T>C NP_958816.1:p.Val717Ala
NM_201414.3:c.1982T>C NP_958817.1:p.Val661Ala
NM_001136131.3:c.1877T>C NP_001129603.1:p.Val626Ala
NM_001385253.1:c.2039T>C NP_001372182.1:p.Val680Ala