Canonical Allele Identifier: CA511686009

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27264115A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891803A>C , CM000683.2:g.25891803A>C	GRCh38
NC_000021.8:g.27264115A>C , CM000683.1:g.27264115A>C	GRCh37
NC_000021.7:g.26185986A>C	NCBI36
NG_007376.1:g.284018T>G
NG_007376.2:g.284326T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2097T>G
ENST00000707133.1:n.527T>G
ENST00000707134.1:n.796T>G
ENST00000346798.8:c.2130T>G MANE Select	ENSP00000284981.4:p.Val710=
ENST00000346798.7:c.2130T>G	ENSP00000284981.4:p.Val710=
ENST00000348990.9:c.1905T>G	ENSP00000345463.5:p.Val635=
ENST00000354192.7:c.1737T>G	ENSP00000346129.3:p.Val579=
ENST00000357903.7:c.2073T>G	ENSP00000350578.3:p.Val691=
ENST00000358918.7:c.2076T>G	ENSP00000351796.3:p.Val692=
ENST00000359726.7:c.1800T>G	ENSP00000352760.4:p.Val600=
ENST00000439274.6:c.1962T>G	ENSP00000398879.2:p.Val654=
ENST00000440126.7:c.2058T>G	ENSP00000387483.2:p.Val686=
ENST00000464867.1:n.477T>G
NM_000484.3:c.2130T>G	NP_000475.1:p.Val710=
NM_001136016.3:c.2058T>G	NP_001129488.1:p.Val686=
NM_001136129.2:c.1737T>G	NP_001129601.1:p.Val579=
NM_001136130.2:c.1962T>G	NP_001129602.1:p.Val654=
NM_001136131.2:c.1800T>G	NP_001129603.1:p.Val600=
NM_001204301.1:c.2076T>G	NP_001191230.1:p.Val692=
NM_001204302.1:c.2019T>G	NP_001191231.1:p.Val673=
NM_001204303.1:c.1851T>G	NP_001191232.1:p.Val617=
NM_201413.2:c.2073T>G	NP_958816.1:p.Val691=
NM_201414.2:c.1905T>G	NP_958817.1:p.Val635=
NM_000484.4:c.2130T>G MANE Select	NP_000475.1:p.Val710=
NM_001136129.3:c.1737T>G	NP_001129601.1:p.Val579=
NM_001136130.3:c.1962T>G	NP_001129602.1:p.Val654=
NM_001204301.2:c.2076T>G	NP_001191230.1:p.Val692=
NM_001204302.2:c.2019T>G	NP_001191231.1:p.Val673=
NM_001204303.2:c.1851T>G	NP_001191232.1:p.Val617=
NM_201413.3:c.2073T>G	NP_958816.1:p.Val691=
NM_201414.3:c.1905T>G	NP_958817.1:p.Val635=
NM_001136131.3:c.1800T>G	NP_001129603.1:p.Val600=
NM_001385253.1:c.1962T>G	NP_001372182.1:p.Val654=