Canonical Allele Identifier: CA409805418

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891724C>T , CM000683.2:g.25891724C>T	GRCh38
NC_000021.8:g.27264036C>T , CM000683.1:g.27264036C>T	GRCh37
NC_000021.7:g.26185907C>T	NCBI36
NG_007376.1:g.284097G>A
NG_007376.2:g.284405G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000484.4:c.2209G>A MANE Select	NP_000475.1:p.Glu737Lys
ENST00000346798.8:c.2209G>A MANE Select	ENSP00000284981.4:p.Glu737Lys
NM_000484.3:c.2209G>A	NP_000475.1:p.Glu737Lys
NM_001136016.3:c.2137G>A	NP_001129488.1:p.Glu713Lys
NM_001136129.2:c.1816G>A	NP_001129601.1:p.Glu606Lys
NM_001136129.3:c.1816G>A	NP_001129601.1:p.Glu606Lys
NM_001136130.2:c.2041G>A	NP_001129602.1:p.Glu681Lys
NM_001136130.3:c.2041G>A	NP_001129602.1:p.Glu681Lys
NM_001136131.2:c.1879G>A	NP_001129603.1:p.Glu627Lys
NM_001136131.3:c.1879G>A	NP_001129603.1:p.Glu627Lys
NM_001204301.1:c.2155G>A	NP_001191230.1:p.Glu719Lys
NM_001204301.2:c.2155G>A	NP_001191230.1:p.Glu719Lys
NM_001204302.1:c.2098G>A	NP_001191231.1:p.Glu700Lys
NM_001204302.2:c.2098G>A	NP_001191231.1:p.Glu700Lys
NM_001204303.1:c.1930G>A	NP_001191232.1:p.Glu644Lys
NM_001204303.2:c.1930G>A	NP_001191232.1:p.Glu644Lys
NM_001385253.1:c.2041G>A	NP_001372182.1:p.Glu681Lys
NM_201413.2:c.2152G>A	NP_958816.1:p.Glu718Lys
NM_201413.3:c.2152G>A	NP_958816.1:p.Glu718Lys
NM_201414.2:c.1984G>A	NP_958817.1:p.Glu662Lys
NM_201414.3:c.1984G>A	NP_958817.1:p.Glu662Lys
ENST00000346798.7:c.2209G>A	ENSP00000284981.4:p.Glu737Lys
ENST00000348990.9:c.1984G>A	ENSP00000345463.5:p.Glu662Lys
ENST00000354192.7:c.1816G>A	ENSP00000346129.3:p.Glu606Lys
ENST00000357903.7:c.2152G>A	ENSP00000350578.3:p.Glu718Lys
ENST00000358918.7:c.2155G>A	ENSP00000351796.3:p.Glu719Lys
ENST00000359726.7:c.1879G>A	ENSP00000352760.4:p.Glu627Lys
ENST00000439274.6:c.2041G>A	ENSP00000398879.2:p.Glu681Lys
ENST00000440126.7:c.2137G>A	ENSP00000387483.2:p.Glu713Lys
ENST00000464867.1:n.556G>A
ENST00000707132.1:n.2176G>A
ENST00000707133.1:n.606G>A
ENST00000707134.1:n.875G>A