Canonical Allele Identifier: CA409805419
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2207T>G MANE Select ENSP00000284981.4:p.Val736Gly
ENST00000346798.7:c.2207T>G ENSP00000284981.4:p.Val736Gly
ENST00000348990.9:c.1982T>G ENSP00000345463.5:p.Val661Gly
ENST00000354192.7:c.1814T>G ENSP00000346129.3:p.Val605Gly
ENST00000357903.7:c.2150T>G ENSP00000350578.3:p.Val717Gly
ENST00000358918.7:c.2153T>G ENSP00000351796.3:p.Val718Gly
ENST00000359726.7:c.1877T>G ENSP00000352760.4:p.Val626Gly
ENST00000439274.6:c.2039T>G ENSP00000398879.2:p.Val680Gly
ENST00000440126.7:c.2135T>G ENSP00000387483.2:p.Val712Gly
ENST00000464867.1:n.554T>G
NM_000484.3:c.2207T>G NP_000475.1:p.Val736Gly
NM_001136016.3:c.2135T>G NP_001129488.1:p.Val712Gly
NM_001136129.2:c.1814T>G NP_001129601.1:p.Val605Gly
NM_001136130.2:c.2039T>G NP_001129602.1:p.Val680Gly
NM_001136131.2:c.1877T>G NP_001129603.1:p.Val626Gly
NM_001204301.1:c.2153T>G NP_001191230.1:p.Val718Gly
NM_001204302.1:c.2096T>G NP_001191231.1:p.Val699Gly
NM_001204303.1:c.1928T>G NP_001191232.1:p.Val643Gly
NM_201413.2:c.2150T>G NP_958816.1:p.Val717Gly
NM_201414.2:c.1982T>G NP_958817.1:p.Val661Gly
NM_000484.4:c.2207T>G MANE Select NP_000475.1:p.Val736Gly
NM_001136129.3:c.1814T>G NP_001129601.1:p.Val605Gly
NM_001136130.3:c.2039T>G NP_001129602.1:p.Val680Gly
NM_001204301.2:c.2153T>G NP_001191230.1:p.Val718Gly
NM_001204302.2:c.2096T>G NP_001191231.1:p.Val699Gly
NM_001204303.2:c.1928T>G NP_001191232.1:p.Val643Gly
NM_201413.3:c.2150T>G NP_958816.1:p.Val717Gly
NM_201414.3:c.1982T>G NP_958817.1:p.Val661Gly
NM_001136131.3:c.1877T>G NP_001129603.1:p.Val626Gly
NM_001385253.1:c.2039T>G NP_001372182.1:p.Val680Gly