Canonical Allele Identifier: CA511686175

Gene: APP

Linked Data

• gnomAD v4: 21-25897611-G-T
• MyVariant Identifiers: chr21:g.27269923G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897611G>T , CM000683.2:g.25897611G>T	GRCh38
NC_000021.8:g.27269923G>T , CM000683.1:g.27269923G>T	GRCh37
NC_000021.7:g.26191794G>T	NCBI36
NG_007376.1:g.278210C>A
NG_007376.2:g.278518C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1993C>A
ENST00000707133.1:n.423C>A
ENST00000707134.1:n.692C>A
ENST00000346798.8:c.2026C>A MANE Select	ENSP00000284981.4:p.Arg676=
ENST00000346798.7:c.2026C>A	ENSP00000284981.4:p.Arg676=
ENST00000348990.9:c.1801C>A	ENSP00000345463.5:p.Arg601=
ENST00000354192.7:c.1633C>A	ENSP00000346129.3:p.Arg545=
ENST00000357903.7:c.1969C>A	ENSP00000350578.3:p.Arg657=
ENST00000358918.7:c.1972C>A	ENSP00000351796.3:p.Arg658=
ENST00000359726.7:c.1696C>A	ENSP00000352760.4:p.Arg566=
ENST00000439274.6:c.1858C>A	ENSP00000398879.2:p.Arg620=
ENST00000440126.7:c.1954C>A	ENSP00000387483.2:p.Arg652=
ENST00000464867.1:n.373C>A
NM_000484.3:c.2026C>A	NP_000475.1:p.Arg676=
NM_001136016.3:c.1954C>A	NP_001129488.1:p.Arg652=
NM_001136129.2:c.1633C>A	NP_001129601.1:p.Arg545=
NM_001136130.2:c.1858C>A	NP_001129602.1:p.Arg620=
NM_001136131.2:c.1696C>A	NP_001129603.1:p.Arg566=
NM_001204301.1:c.1972C>A	NP_001191230.1:p.Arg658=
NM_001204302.1:c.1915C>A	NP_001191231.1:p.Arg639=
NM_001204303.1:c.1747C>A	NP_001191232.1:p.Arg583=
NM_201413.2:c.1969C>A	NP_958816.1:p.Arg657=
NM_201414.2:c.1801C>A	NP_958817.1:p.Arg601=
NM_000484.4:c.2026C>A MANE Select	NP_000475.1:p.Arg676=
NM_001136129.3:c.1633C>A	NP_001129601.1:p.Arg545=
NM_001136130.3:c.1858C>A	NP_001129602.1:p.Arg620=
NM_001204301.2:c.1972C>A	NP_001191230.1:p.Arg658=
NM_001204302.2:c.1915C>A	NP_001191231.1:p.Arg639=
NM_001204303.2:c.1747C>A	NP_001191232.1:p.Arg583=
NM_201413.3:c.1969C>A	NP_958816.1:p.Arg657=
NM_201414.3:c.1801C>A	NP_958817.1:p.Arg601=
NM_001136131.3:c.1696C>A	NP_001129603.1:p.Arg566=
NM_001385253.1:c.1858C>A	NP_001372182.1:p.Arg620=