Canonical Allele Identifier: CA409805517
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891767C>T , CM000683.2:g.25891767C>T GRCh38
NC_000021.8:g.27264079C>T , CM000683.1:g.27264079C>T GRCh37
NC_000021.7:g.26185950C>T NCBI36
NG_007376.1:g.284054G>A
NG_007376.2:g.284362G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2166G>A MANE Select ENSP00000284981.4:p.Met722Ile
ENST00000346798.7:c.2166G>A ENSP00000284981.4:p.Met722Ile
ENST00000348990.9:c.1941G>A ENSP00000345463.5:p.Met647Ile
ENST00000354192.7:c.1773G>A ENSP00000346129.3:p.Met591Ile
ENST00000357903.7:c.2109G>A ENSP00000350578.3:p.Met703Ile
ENST00000358918.7:c.2112G>A ENSP00000351796.3:p.Met704Ile
ENST00000359726.7:c.1836G>A ENSP00000352760.4:p.Met612Ile
ENST00000439274.6:c.1998G>A ENSP00000398879.2:p.Met666Ile
ENST00000440126.7:c.2094G>A ENSP00000387483.2:p.Met698Ile
ENST00000464867.1:n.513G>A
NM_000484.3:c.2166G>A NP_000475.1:p.Met722Ile
NM_001136016.3:c.2094G>A NP_001129488.1:p.Met698Ile
NM_001136129.2:c.1773G>A NP_001129601.1:p.Met591Ile
NM_001136130.2:c.1998G>A NP_001129602.1:p.Met666Ile
NM_001136131.2:c.1836G>A NP_001129603.1:p.Met612Ile
NM_001204301.1:c.2112G>A NP_001191230.1:p.Met704Ile
NM_001204302.1:c.2055G>A NP_001191231.1:p.Met685Ile
NM_001204303.1:c.1887G>A NP_001191232.1:p.Met629Ile
NM_201413.2:c.2109G>A NP_958816.1:p.Met703Ile
NM_201414.2:c.1941G>A NP_958817.1:p.Met647Ile
NM_000484.4:c.2166G>A MANE Select NP_000475.1:p.Met722Ile
NM_001136129.3:c.1773G>A NP_001129601.1:p.Met591Ile
NM_001136130.3:c.1998G>A NP_001129602.1:p.Met666Ile
NM_001204301.2:c.2112G>A NP_001191230.1:p.Met704Ile
NM_001204302.2:c.2055G>A NP_001191231.1:p.Met685Ile
NM_001204303.2:c.1887G>A NP_001191232.1:p.Met629Ile
NM_201413.3:c.2109G>A NP_958816.1:p.Met703Ile
NM_201414.3:c.1941G>A NP_958817.1:p.Met647Ile
NM_001136131.3:c.1836G>A NP_001129603.1:p.Met612Ile
NM_001385253.1:c.1998G>A NP_001372182.1:p.Met666Ile