Canonical Allele Identifier: CA409805512

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27264077A>T (hg19) ; chr21:g.25891765A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891765A>T , CM000683.2:g.25891765A>T	GRCh38
NC_000021.8:g.27264077A>T , CM000683.1:g.27264077A>T	GRCh37
NC_000021.7:g.26185948A>T	NCBI36
NG_007376.1:g.284056T>A
NG_007376.2:g.284364T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2135T>A
ENST00000707133.1:n.565T>A
ENST00000707134.1:n.834T>A
ENST00000346798.8:c.2168T>A MANE Select	ENSP00000284981.4:p.Leu723Gln
ENST00000346798.7:c.2168T>A	ENSP00000284981.4:p.Leu723Gln
ENST00000348990.9:c.1943T>A	ENSP00000345463.5:p.Leu648Gln
ENST00000354192.7:c.1775T>A	ENSP00000346129.3:p.Leu592Gln
ENST00000357903.7:c.2111T>A	ENSP00000350578.3:p.Leu704Gln
ENST00000358918.7:c.2114T>A	ENSP00000351796.3:p.Leu705Gln
ENST00000359726.7:c.1838T>A	ENSP00000352760.4:p.Leu613Gln
ENST00000439274.6:c.2000T>A	ENSP00000398879.2:p.Leu667Gln
ENST00000440126.7:c.2096T>A	ENSP00000387483.2:p.Leu699Gln
ENST00000464867.1:n.515T>A
NM_000484.3:c.2168T>A	NP_000475.1:p.Leu723Gln
NM_001136016.3:c.2096T>A	NP_001129488.1:p.Leu699Gln
NM_001136129.2:c.1775T>A	NP_001129601.1:p.Leu592Gln
NM_001136130.2:c.2000T>A	NP_001129602.1:p.Leu667Gln
NM_001136131.2:c.1838T>A	NP_001129603.1:p.Leu613Gln
NM_001204301.1:c.2114T>A	NP_001191230.1:p.Leu705Gln
NM_001204302.1:c.2057T>A	NP_001191231.1:p.Leu686Gln
NM_001204303.1:c.1889T>A	NP_001191232.1:p.Leu630Gln
NM_201413.2:c.2111T>A	NP_958816.1:p.Leu704Gln
NM_201414.2:c.1943T>A	NP_958817.1:p.Leu648Gln
NM_000484.4:c.2168T>A MANE Select	NP_000475.1:p.Leu723Gln
NM_001136129.3:c.1775T>A	NP_001129601.1:p.Leu592Gln
NM_001136130.3:c.2000T>A	NP_001129602.1:p.Leu667Gln
NM_001204301.2:c.2114T>A	NP_001191230.1:p.Leu705Gln
NM_001204302.2:c.2057T>A	NP_001191231.1:p.Leu686Gln
NM_001204303.2:c.1889T>A	NP_001191232.1:p.Leu630Gln
NM_201413.3:c.2111T>A	NP_958816.1:p.Leu704Gln
NM_201414.3:c.1943T>A	NP_958817.1:p.Leu648Gln
NM_001136131.3:c.1838T>A	NP_001129603.1:p.Leu613Gln
NM_001385253.1:c.2000T>A	NP_001372182.1:p.Leu667Gln