Canonical Allele Identifier: CA409806310
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897594A>C , CM000683.2:g.25897594A>C GRCh38
NC_000021.8:g.27269906A>C , CM000683.1:g.27269906A>C GRCh37
NC_000021.7:g.26191777A>C NCBI36
NG_007376.1:g.278227T>G
NG_007376.2:g.278535T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2010T>G
ENST00000707133.1:n.440T>G
ENST00000707134.1:n.709T>G
ENST00000346798.8:c.2043T>G MANE Select ENSP00000284981.4:p.Tyr681Ter
ENST00000346798.7:c.2043T>G ENSP00000284981.4:p.Tyr681Ter
ENST00000348990.9:c.1818T>G ENSP00000345463.5:p.Tyr606Ter
ENST00000354192.7:c.1650T>G ENSP00000346129.3:p.Tyr550Ter
ENST00000357903.7:c.1986T>G ENSP00000350578.3:p.Tyr662Ter
ENST00000358918.7:c.1989T>G ENSP00000351796.3:p.Tyr663Ter
ENST00000359726.7:c.1713T>G ENSP00000352760.4:p.Tyr571Ter
ENST00000439274.6:c.1875T>G ENSP00000398879.2:p.Tyr625Ter
ENST00000440126.7:c.1971T>G ENSP00000387483.2:p.Tyr657Ter
ENST00000464867.1:n.390T>G
NM_000484.3:c.2043T>G NP_000475.1:p.Tyr681Ter
NM_001136016.3:c.1971T>G NP_001129488.1:p.Tyr657Ter
NM_001136129.2:c.1650T>G NP_001129601.1:p.Tyr550Ter
NM_001136130.2:c.1875T>G NP_001129602.1:p.Tyr625Ter
NM_001136131.2:c.1713T>G NP_001129603.1:p.Tyr571Ter
NM_001204301.1:c.1989T>G NP_001191230.1:p.Tyr663Ter
NM_001204302.1:c.1932T>G NP_001191231.1:p.Tyr644Ter
NM_001204303.1:c.1764T>G NP_001191232.1:p.Tyr588Ter
NM_201413.2:c.1986T>G NP_958816.1:p.Tyr662Ter
NM_201414.2:c.1818T>G NP_958817.1:p.Tyr606Ter
NM_000484.4:c.2043T>G MANE Select NP_000475.1:p.Tyr681Ter
NM_001136129.3:c.1650T>G NP_001129601.1:p.Tyr550Ter
NM_001136130.3:c.1875T>G NP_001129602.1:p.Tyr625Ter
NM_001204301.2:c.1989T>G NP_001191230.1:p.Tyr663Ter
NM_001204302.2:c.1932T>G NP_001191231.1:p.Tyr644Ter
NM_001204303.2:c.1764T>G NP_001191232.1:p.Tyr588Ter
NM_201413.3:c.1986T>G NP_958816.1:p.Tyr662Ter
NM_201414.3:c.1818T>G NP_958817.1:p.Tyr606Ter
NM_001136131.3:c.1713T>G NP_001129603.1:p.Tyr571Ter
NM_001385253.1:c.1875T>G NP_001372182.1:p.Tyr625Ter