Canonical Allele Identifier: CA409805608
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891817T>C , CM000683.2:g.25891817T>C GRCh38
NC_000021.8:g.27264129T>C , CM000683.1:g.27264129T>C GRCh37
NC_000021.7:g.26186000T>C NCBI36
NG_007376.1:g.284004A>G
NG_007376.2:g.284312A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2083A>G
ENST00000707133.1:n.513A>G
ENST00000707134.1:n.782A>G
ENST00000346798.8:c.2116A>G MANE Select ENSP00000284981.4:p.Met706Val
ENST00000346798.7:c.2116A>G ENSP00000284981.4:p.Met706Val
ENST00000348990.9:c.1891A>G ENSP00000345463.5:p.Met631Val
ENST00000354192.7:c.1723A>G ENSP00000346129.3:p.Met575Val
ENST00000357903.7:c.2059A>G ENSP00000350578.3:p.Met687Val
ENST00000358918.7:c.2062A>G ENSP00000351796.3:p.Met688Val
ENST00000359726.7:c.1786A>G ENSP00000352760.4:p.Met596Val
ENST00000439274.6:c.1948A>G ENSP00000398879.2:p.Met650Val
ENST00000440126.7:c.2044A>G ENSP00000387483.2:p.Met682Val
ENST00000464867.1:n.463A>G
NM_000484.3:c.2116A>G NP_000475.1:p.Met706Val
NM_001136016.3:c.2044A>G NP_001129488.1:p.Met682Val
NM_001136129.2:c.1723A>G NP_001129601.1:p.Met575Val
NM_001136130.2:c.1948A>G NP_001129602.1:p.Met650Val
NM_001136131.2:c.1786A>G NP_001129603.1:p.Met596Val
NM_001204301.1:c.2062A>G NP_001191230.1:p.Met688Val
NM_001204302.1:c.2005A>G NP_001191231.1:p.Met669Val
NM_001204303.1:c.1837A>G NP_001191232.1:p.Met613Val
NM_201413.2:c.2059A>G NP_958816.1:p.Met687Val
NM_201414.2:c.1891A>G NP_958817.1:p.Met631Val
NM_000484.4:c.2116A>G MANE Select NP_000475.1:p.Met706Val
NM_001136129.3:c.1723A>G NP_001129601.1:p.Met575Val
NM_001136130.3:c.1948A>G NP_001129602.1:p.Met650Val
NM_001204301.2:c.2062A>G NP_001191230.1:p.Met688Val
NM_001204302.2:c.2005A>G NP_001191231.1:p.Met669Val
NM_001204303.2:c.1837A>G NP_001191232.1:p.Met613Val
NM_201413.3:c.2059A>G NP_958816.1:p.Met687Val
NM_201414.3:c.1891A>G NP_958817.1:p.Met631Val
NM_001136131.3:c.1786A>G NP_001129603.1:p.Met596Val
NM_001385253.1:c.1948A>G NP_001372182.1:p.Met650Val