Canonical Allele Identifier: CA409805514

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27264078G>T (hg19) ; chr21:g.25891766G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891766G>T , CM000683.2:g.25891766G>T	GRCh38
NC_000021.8:g.27264078G>T , CM000683.1:g.27264078G>T	GRCh37
NC_000021.7:g.26185949G>T	NCBI36
NG_007376.1:g.284055C>A
NG_007376.2:g.284363C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2134C>A
ENST00000707133.1:n.564C>A
ENST00000707134.1:n.833C>A
ENST00000346798.8:c.2167C>A MANE Select	ENSP00000284981.4:p.Leu723Met
ENST00000346798.7:c.2167C>A	ENSP00000284981.4:p.Leu723Met
ENST00000348990.9:c.1942C>A	ENSP00000345463.5:p.Leu648Met
ENST00000354192.7:c.1774C>A	ENSP00000346129.3:p.Leu592Met
ENST00000357903.7:c.2110C>A	ENSP00000350578.3:p.Leu704Met
ENST00000358918.7:c.2113C>A	ENSP00000351796.3:p.Leu705Met
ENST00000359726.7:c.1837C>A	ENSP00000352760.4:p.Leu613Met
ENST00000439274.6:c.1999C>A	ENSP00000398879.2:p.Leu667Met
ENST00000440126.7:c.2095C>A	ENSP00000387483.2:p.Leu699Met
ENST00000464867.1:n.514C>A
NM_000484.3:c.2167C>A	NP_000475.1:p.Leu723Met
NM_001136016.3:c.2095C>A	NP_001129488.1:p.Leu699Met
NM_001136129.2:c.1774C>A	NP_001129601.1:p.Leu592Met
NM_001136130.2:c.1999C>A	NP_001129602.1:p.Leu667Met
NM_001136131.2:c.1837C>A	NP_001129603.1:p.Leu613Met
NM_001204301.1:c.2113C>A	NP_001191230.1:p.Leu705Met
NM_001204302.1:c.2056C>A	NP_001191231.1:p.Leu686Met
NM_001204303.1:c.1888C>A	NP_001191232.1:p.Leu630Met
NM_201413.2:c.2110C>A	NP_958816.1:p.Leu704Met
NM_201414.2:c.1942C>A	NP_958817.1:p.Leu648Met
NM_000484.4:c.2167C>A MANE Select	NP_000475.1:p.Leu723Met
NM_001136129.3:c.1774C>A	NP_001129601.1:p.Leu592Met
NM_001136130.3:c.1999C>A	NP_001129602.1:p.Leu667Met
NM_001204301.2:c.2113C>A	NP_001191230.1:p.Leu705Met
NM_001204302.2:c.2056C>A	NP_001191231.1:p.Leu686Met
NM_001204303.2:c.1888C>A	NP_001191232.1:p.Leu630Met
NM_201413.3:c.2110C>A	NP_958816.1:p.Leu704Met
NM_201414.3:c.1942C>A	NP_958817.1:p.Leu648Met
NM_001136131.3:c.1837C>A	NP_001129603.1:p.Leu613Met
NM_001385253.1:c.1999C>A	NP_001372182.1:p.Leu667Met