Canonical Allele Identifier: CA511686361

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27269972T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897660T>A , CM000683.2:g.25897660T>A	GRCh38
NC_000021.8:g.27269972T>A , CM000683.1:g.27269972T>A	GRCh37
NC_000021.7:g.26191843T>A	NCBI36
NG_007376.1:g.278161A>T
NG_007376.2:g.278469A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.1944A>T
ENST00000707133.1:n.374A>T
ENST00000707134.1:n.643A>T
ENST00000346798.8:c.1977A>T MANE Select	ENSP00000284981.4:p.Thr659=
ENST00000346798.7:c.1977A>T	ENSP00000284981.4:p.Thr659=
ENST00000348990.9:c.1752A>T	ENSP00000345463.5:p.Thr584=
ENST00000354192.7:c.1584A>T	ENSP00000346129.3:p.Thr528=
ENST00000357903.7:c.1920A>T	ENSP00000350578.3:p.Thr640=
ENST00000358918.7:c.1923A>T	ENSP00000351796.3:p.Thr641=
ENST00000359726.7:c.1647A>T	ENSP00000352760.4:p.Thr549=
ENST00000439274.6:c.1809A>T	ENSP00000398879.2:p.Thr603=
ENST00000440126.7:c.1905A>T	ENSP00000387483.2:p.Thr635=
ENST00000464867.1:n.324A>T
NM_000484.3:c.1977A>T	NP_000475.1:p.Thr659=
NM_001136016.3:c.1905A>T	NP_001129488.1:p.Thr635=
NM_001136129.2:c.1584A>T	NP_001129601.1:p.Thr528=
NM_001136130.2:c.1809A>T	NP_001129602.1:p.Thr603=
NM_001136131.2:c.1647A>T	NP_001129603.1:p.Thr549=
NM_001204301.1:c.1923A>T	NP_001191230.1:p.Thr641=
NM_001204302.1:c.1866A>T	NP_001191231.1:p.Thr622=
NM_001204303.1:c.1698A>T	NP_001191232.1:p.Thr566=
NM_201413.2:c.1920A>T	NP_958816.1:p.Thr640=
NM_201414.2:c.1752A>T	NP_958817.1:p.Thr584=
NM_000484.4:c.1977A>T MANE Select	NP_000475.1:p.Thr659=
NM_001136129.3:c.1584A>T	NP_001129601.1:p.Thr528=
NM_001136130.3:c.1809A>T	NP_001129602.1:p.Thr603=
NM_001204301.2:c.1923A>T	NP_001191230.1:p.Thr641=
NM_001204302.2:c.1866A>T	NP_001191231.1:p.Thr622=
NM_001204303.2:c.1698A>T	NP_001191232.1:p.Thr566=
NM_201413.3:c.1920A>T	NP_958816.1:p.Thr640=
NM_201414.3:c.1752A>T	NP_958817.1:p.Thr584=
NM_001136131.3:c.1647A>T	NP_001129603.1:p.Thr549=
NM_001385253.1:c.1809A>T	NP_001372182.1:p.Thr603=