Canonical Allele Identifier: CA409805422
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891727C>T , CM000683.2:g.25891727C>T GRCh38
NC_000021.8:g.27264039C>T , CM000683.1:g.27264039C>T GRCh37
NC_000021.7:g.26185910C>T NCBI36
NG_007376.1:g.284094G>A
NG_007376.2:g.284402G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2206G>A MANE Select ENSP00000284981.4:p.Val736Met
ENST00000346798.7:c.2206G>A ENSP00000284981.4:p.Val736Met
ENST00000348990.9:c.1981G>A ENSP00000345463.5:p.Val661Met
ENST00000354192.7:c.1813G>A ENSP00000346129.3:p.Val605Met
ENST00000357903.7:c.2149G>A ENSP00000350578.3:p.Val717Met
ENST00000358918.7:c.2152G>A ENSP00000351796.3:p.Val718Met
ENST00000359726.7:c.1876G>A ENSP00000352760.4:p.Val626Met
ENST00000439274.6:c.2038G>A ENSP00000398879.2:p.Val680Met
ENST00000440126.7:c.2134G>A ENSP00000387483.2:p.Val712Met
ENST00000464867.1:n.553G>A
NM_000484.3:c.2206G>A NP_000475.1:p.Val736Met
NM_001136016.3:c.2134G>A NP_001129488.1:p.Val712Met
NM_001136129.2:c.1813G>A NP_001129601.1:p.Val605Met
NM_001136130.2:c.2038G>A NP_001129602.1:p.Val680Met
NM_001136131.2:c.1876G>A NP_001129603.1:p.Val626Met
NM_001204301.1:c.2152G>A NP_001191230.1:p.Val718Met
NM_001204302.1:c.2095G>A NP_001191231.1:p.Val699Met
NM_001204303.1:c.1927G>A NP_001191232.1:p.Val643Met
NM_201413.2:c.2149G>A NP_958816.1:p.Val717Met
NM_201414.2:c.1981G>A NP_958817.1:p.Val661Met
NM_000484.4:c.2206G>A MANE Select NP_000475.1:p.Val736Met
NM_001136129.3:c.1813G>A NP_001129601.1:p.Val605Met
NM_001136130.3:c.2038G>A NP_001129602.1:p.Val680Met
NM_001204301.2:c.2152G>A NP_001191230.1:p.Val718Met
NM_001204302.2:c.2095G>A NP_001191231.1:p.Val699Met
NM_001204303.2:c.1927G>A NP_001191232.1:p.Val643Met
NM_201413.3:c.2149G>A NP_958816.1:p.Val717Met
NM_201414.3:c.1981G>A NP_958817.1:p.Val661Met
NM_001136131.3:c.1876G>A NP_001129603.1:p.Val626Met
NM_001385253.1:c.2038G>A NP_001372182.1:p.Val680Met