Canonical Allele Identifier: CA319103543
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs564935101

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897648C>T , CM000683.2:g.25897648C>T GRCh38
NC_000021.8:g.27269960C>T , CM000683.1:g.27269960C>T GRCh37
NC_000021.7:g.26191831C>T NCBI36
NG_007376.1:g.278173G>A
NG_007376.2:g.278481G>A

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.1989G>A NP_000475.1:p.Thr663=
NM_001136016.3:c.1917G>A NP_001129488.1:p.Thr639=
NM_001136129.2:c.1596G>A NP_001129601.1:p.Thr532=
NM_001136130.2:c.1821G>A NP_001129602.1:p.Thr607=
NM_001136131.2:c.1659G>A NP_001129603.1:p.Thr553=
NM_001204301.1:c.1935G>A NP_001191230.1:p.Thr645=
NM_001204302.1:c.1878G>A NP_001191231.1:p.Thr626=
NM_001204303.1:c.1710G>A NP_001191232.1:p.Thr570=
NM_201413.2:c.1932G>A NP_958816.1:p.Thr644=
NM_201414.2:c.1764G>A NP_958817.1:p.Thr588=
NM_000484.4:c.1989G>A MANE Select NP_000475.1:p.Thr663=
NM_001136129.3:c.1596G>A NP_001129601.1:p.Thr532=
NM_001136130.3:c.1821G>A NP_001129602.1:p.Thr607=
NM_001204301.2:c.1935G>A NP_001191230.1:p.Thr645=
NM_001204302.2:c.1878G>A NP_001191231.1:p.Thr626=
NM_001204303.2:c.1710G>A NP_001191232.1:p.Thr570=
NM_201413.3:c.1932G>A NP_958816.1:p.Thr644=
NM_201414.3:c.1764G>A NP_958817.1:p.Thr588=
NM_001136131.3:c.1659G>A NP_001129603.1:p.Thr553=
NM_001385253.1:c.1821G>A NP_001372182.1:p.Thr607=
ENST00000346798.7:c.1989G>A ENSP00000284981.4:p.Thr663=
ENST00000348990.9:c.1764G>A ENSP00000345463.5:p.Thr588=
ENST00000354192.7:c.1596G>A ENSP00000346129.3:p.Thr532=
ENST00000357903.7:c.1932G>A ENSP00000350578.3:p.Thr644=
ENST00000358918.7:c.1935G>A ENSP00000351796.3:p.Thr645=
ENST00000359726.7:c.1659G>A ENSP00000352760.4:p.Thr553=
ENST00000439274.6:c.1821G>A ENSP00000398879.2:p.Thr607=
ENST00000440126.7:c.1917G>A ENSP00000387483.2:p.Thr639=
ENST00000464867.1:n.336G>A