Canonical Allele Identifier: CA409806569

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27269973G>C (hg19) ; chr21:g.25897661G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897661G>C , CM000683.2:g.25897661G>C	GRCh38
NC_000021.8:g.27269973G>C , CM000683.1:g.27269973G>C	GRCh37
NC_000021.7:g.26191844G>C	NCBI36
NG_007376.1:g.278160C>G
NG_007376.2:g.278468C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.1943C>G
ENST00000707133.1:n.373C>G
ENST00000707134.1:n.642C>G
ENST00000346798.8:c.1976C>G MANE Select	ENSP00000284981.4:p.Thr659Arg
ENST00000346798.7:c.1976C>G	ENSP00000284981.4:p.Thr659Arg
ENST00000348990.9:c.1751C>G	ENSP00000345463.5:p.Thr584Arg
ENST00000354192.7:c.1583C>G	ENSP00000346129.3:p.Thr528Arg
ENST00000357903.7:c.1919C>G	ENSP00000350578.3:p.Thr640Arg
ENST00000358918.7:c.1922C>G	ENSP00000351796.3:p.Thr641Arg
ENST00000359726.7:c.1646C>G	ENSP00000352760.4:p.Thr549Arg
ENST00000439274.6:c.1808C>G	ENSP00000398879.2:p.Thr603Arg
ENST00000440126.7:c.1904C>G	ENSP00000387483.2:p.Thr635Arg
ENST00000464867.1:n.323C>G
NM_000484.3:c.1976C>G	NP_000475.1:p.Thr659Arg
NM_001136016.3:c.1904C>G	NP_001129488.1:p.Thr635Arg
NM_001136129.2:c.1583C>G	NP_001129601.1:p.Thr528Arg
NM_001136130.2:c.1808C>G	NP_001129602.1:p.Thr603Arg
NM_001136131.2:c.1646C>G	NP_001129603.1:p.Thr549Arg
NM_001204301.1:c.1922C>G	NP_001191230.1:p.Thr641Arg
NM_001204302.1:c.1865C>G	NP_001191231.1:p.Thr622Arg
NM_001204303.1:c.1697C>G	NP_001191232.1:p.Thr566Arg
NM_201413.2:c.1919C>G	NP_958816.1:p.Thr640Arg
NM_201414.2:c.1751C>G	NP_958817.1:p.Thr584Arg
NM_000484.4:c.1976C>G MANE Select	NP_000475.1:p.Thr659Arg
NM_001136129.3:c.1583C>G	NP_001129601.1:p.Thr528Arg
NM_001136130.3:c.1808C>G	NP_001129602.1:p.Thr603Arg
NM_001204301.2:c.1922C>G	NP_001191230.1:p.Thr641Arg
NM_001204302.2:c.1865C>G	NP_001191231.1:p.Thr622Arg
NM_001204303.2:c.1697C>G	NP_001191232.1:p.Thr566Arg
NM_201413.3:c.1919C>G	NP_958816.1:p.Thr640Arg
NM_201414.3:c.1751C>G	NP_958817.1:p.Thr584Arg
NM_001136131.3:c.1646C>G	NP_001129603.1:p.Thr549Arg
NM_001385253.1:c.1808C>G	NP_001372182.1:p.Thr603Arg