Canonical Allele Identifier: CA409806258
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897583T>A , CM000683.2:g.25897583T>A GRCh38
NC_000021.8:g.27269895T>A , CM000683.1:g.27269895T>A GRCh37
NC_000021.7:g.26191766T>A NCBI36
NG_007376.1:g.278238A>T
NG_007376.2:g.278546A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2021A>T
ENST00000707133.1:n.451A>T
ENST00000707134.1:n.720A>T
ENST00000346798.8:c.2054A>T MANE Select ENSP00000284981.4:p.His685Leu
ENST00000346798.7:c.2054A>T ENSP00000284981.4:p.His685Leu
ENST00000348990.9:c.1829A>T ENSP00000345463.5:p.His610Leu
ENST00000354192.7:c.1661A>T ENSP00000346129.3:p.His554Leu
ENST00000357903.7:c.1997A>T ENSP00000350578.3:p.His666Leu
ENST00000358918.7:c.2000A>T ENSP00000351796.3:p.His667Leu
ENST00000359726.7:c.1724A>T ENSP00000352760.4:p.His575Leu
ENST00000439274.6:c.1886A>T ENSP00000398879.2:p.His629Leu
ENST00000440126.7:c.1982A>T ENSP00000387483.2:p.His661Leu
ENST00000464867.1:n.401A>T
NM_000484.3:c.2054A>T NP_000475.1:p.His685Leu
NM_001136016.3:c.1982A>T NP_001129488.1:p.His661Leu
NM_001136129.2:c.1661A>T NP_001129601.1:p.His554Leu
NM_001136130.2:c.1886A>T NP_001129602.1:p.His629Leu
NM_001136131.2:c.1724A>T NP_001129603.1:p.His575Leu
NM_001204301.1:c.2000A>T NP_001191230.1:p.His667Leu
NM_001204302.1:c.1943A>T NP_001191231.1:p.His648Leu
NM_001204303.1:c.1775A>T NP_001191232.1:p.His592Leu
NM_201413.2:c.1997A>T NP_958816.1:p.His666Leu
NM_201414.2:c.1829A>T NP_958817.1:p.His610Leu
NM_000484.4:c.2054A>T MANE Select NP_000475.1:p.His685Leu
NM_001136129.3:c.1661A>T NP_001129601.1:p.His554Leu
NM_001136130.3:c.1886A>T NP_001129602.1:p.His629Leu
NM_001204301.2:c.2000A>T NP_001191230.1:p.His667Leu
NM_001204302.2:c.1943A>T NP_001191231.1:p.His648Leu
NM_001204303.2:c.1775A>T NP_001191232.1:p.His592Leu
NM_201413.3:c.1997A>T NP_958816.1:p.His666Leu
NM_201414.3:c.1829A>T NP_958817.1:p.His610Leu
NM_001136131.3:c.1724A>T NP_001129603.1:p.His575Leu
NM_001385253.1:c.1886A>T NP_001372182.1:p.His629Leu