Canonical Allele Identifier: CA409805446

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27264049A>T (hg19) ; chr21:g.25891737A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891737A>T , CM000683.2:g.25891737A>T	GRCh38
NC_000021.8:g.27264049A>T , CM000683.1:g.27264049A>T	GRCh37
NC_000021.7:g.26185920A>T	NCBI36
NG_007376.1:g.284084T>A
NG_007376.2:g.284392T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2163T>A
ENST00000707133.1:n.593T>A
ENST00000707134.1:n.862T>A
ENST00000346798.8:c.2196T>A MANE Select	ENSP00000284981.4:p.His732Gln
ENST00000346798.7:c.2196T>A	ENSP00000284981.4:p.His732Gln
ENST00000348990.9:c.1971T>A	ENSP00000345463.5:p.His657Gln
ENST00000354192.7:c.1803T>A	ENSP00000346129.3:p.His601Gln
ENST00000357903.7:c.2139T>A	ENSP00000350578.3:p.His713Gln
ENST00000358918.7:c.2142T>A	ENSP00000351796.3:p.His714Gln
ENST00000359726.7:c.1866T>A	ENSP00000352760.4:p.His622Gln
ENST00000439274.6:c.2028T>A	ENSP00000398879.2:p.His676Gln
ENST00000440126.7:c.2124T>A	ENSP00000387483.2:p.His708Gln
ENST00000464867.1:n.543T>A
NM_000484.3:c.2196T>A	NP_000475.1:p.His732Gln
NM_001136016.3:c.2124T>A	NP_001129488.1:p.His708Gln
NM_001136129.2:c.1803T>A	NP_001129601.1:p.His601Gln
NM_001136130.2:c.2028T>A	NP_001129602.1:p.His676Gln
NM_001136131.2:c.1866T>A	NP_001129603.1:p.His622Gln
NM_001204301.1:c.2142T>A	NP_001191230.1:p.His714Gln
NM_001204302.1:c.2085T>A	NP_001191231.1:p.His695Gln
NM_001204303.1:c.1917T>A	NP_001191232.1:p.His639Gln
NM_201413.2:c.2139T>A	NP_958816.1:p.His713Gln
NM_201414.2:c.1971T>A	NP_958817.1:p.His657Gln
NM_000484.4:c.2196T>A MANE Select	NP_000475.1:p.His732Gln
NM_001136129.3:c.1803T>A	NP_001129601.1:p.His601Gln
NM_001136130.3:c.2028T>A	NP_001129602.1:p.His676Gln
NM_001204301.2:c.2142T>A	NP_001191230.1:p.His714Gln
NM_001204302.2:c.2085T>A	NP_001191231.1:p.His695Gln
NM_001204303.2:c.1917T>A	NP_001191232.1:p.His639Gln
NM_201413.3:c.2139T>A	NP_958816.1:p.His713Gln
NM_201414.3:c.1971T>A	NP_958817.1:p.His657Gln
NM_001136131.3:c.1866T>A	NP_001129603.1:p.His622Gln
NM_001385253.1:c.2028T>A	NP_001372182.1:p.His676Gln