Canonical Allele Identifier: CA511686003
Gene: APP HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.27264106C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891794C>A , CM000683.2:g.25891794C>A GRCh38
NC_000021.8:g.27264106C>A , CM000683.1:g.27264106C>A GRCh37
NC_000021.7:g.26185977C>A NCBI36
NG_007376.1:g.284027G>T
NG_007376.2:g.284335G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2106G>T
ENST00000707133.1:n.536G>T
ENST00000707134.1:n.805G>T
ENST00000346798.8:c.2139G>T MANE Select ENSP00000284981.4:p.Ala713=
ENST00000346798.7:c.2139G>T ENSP00000284981.4:p.Ala713=
ENST00000348990.9:c.1914G>T ENSP00000345463.5:p.Ala638=
ENST00000354192.7:c.1746G>T ENSP00000346129.3:p.Ala582=
ENST00000357903.7:c.2082G>T ENSP00000350578.3:p.Ala694=
ENST00000358918.7:c.2085G>T ENSP00000351796.3:p.Ala695=
ENST00000359726.7:c.1809G>T ENSP00000352760.4:p.Ala603=
ENST00000439274.6:c.1971G>T ENSP00000398879.2:p.Ala657=
ENST00000440126.7:c.2067G>T ENSP00000387483.2:p.Ala689=
ENST00000464867.1:n.486G>T
NM_000484.3:c.2139G>T NP_000475.1:p.Ala713=
NM_001136016.3:c.2067G>T NP_001129488.1:p.Ala689=
NM_001136129.2:c.1746G>T NP_001129601.1:p.Ala582=
NM_001136130.2:c.1971G>T NP_001129602.1:p.Ala657=
NM_001136131.2:c.1809G>T NP_001129603.1:p.Ala603=
NM_001204301.1:c.2085G>T NP_001191230.1:p.Ala695=
NM_001204302.1:c.2028G>T NP_001191231.1:p.Ala676=
NM_001204303.1:c.1860G>T NP_001191232.1:p.Ala620=
NM_201413.2:c.2082G>T NP_958816.1:p.Ala694=
NM_201414.2:c.1914G>T NP_958817.1:p.Ala638=
NM_000484.4:c.2139G>T MANE Select NP_000475.1:p.Ala713=
NM_001136129.3:c.1746G>T NP_001129601.1:p.Ala582=
NM_001136130.3:c.1971G>T NP_001129602.1:p.Ala657=
NM_001204301.2:c.2085G>T NP_001191230.1:p.Ala695=
NM_001204302.2:c.2028G>T NP_001191231.1:p.Ala676=
NM_001204303.2:c.1860G>T NP_001191232.1:p.Ala620=
NM_201413.3:c.2082G>T NP_958816.1:p.Ala694=
NM_201414.3:c.1914G>T NP_958817.1:p.Ala638=
NM_001136131.3:c.1809G>T NP_001129603.1:p.Ala603=
NM_001385253.1:c.1971G>T NP_001372182.1:p.Ala657=