Canonical Allele Identifier: CA409805579

Gene: APP

Linked Data

• gnomAD v4: 21-25891802-C-T
• MyVariant Identifiers: chr21:g.27264114C>T (hg19) ; chr21:g.25891802C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891802C>T , CM000683.2:g.25891802C>T	GRCh38
NC_000021.8:g.27264114C>T , CM000683.1:g.27264114C>T	GRCh37
NC_000021.7:g.26185985C>T	NCBI36
NG_007376.1:g.284019G>A
NG_007376.2:g.284327G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2098G>A
ENST00000707133.1:n.528G>A
ENST00000707134.1:n.797G>A
ENST00000346798.8:c.2131G>A MANE Select	ENSP00000284981.4:p.Val711Ile
ENST00000346798.7:c.2131G>A	ENSP00000284981.4:p.Val711Ile
ENST00000348990.9:c.1906G>A	ENSP00000345463.5:p.Val636Ile
ENST00000354192.7:c.1738G>A	ENSP00000346129.3:p.Val580Ile
ENST00000357903.7:c.2074G>A	ENSP00000350578.3:p.Val692Ile
ENST00000358918.7:c.2077G>A	ENSP00000351796.3:p.Val693Ile
ENST00000359726.7:c.1801G>A	ENSP00000352760.4:p.Val601Ile
ENST00000439274.6:c.1963G>A	ENSP00000398879.2:p.Val655Ile
ENST00000440126.7:c.2059G>A	ENSP00000387483.2:p.Val687Ile
ENST00000464867.1:n.478G>A
NM_000484.3:c.2131G>A	NP_000475.1:p.Val711Ile
NM_001136016.3:c.2059G>A	NP_001129488.1:p.Val687Ile
NM_001136129.2:c.1738G>A	NP_001129601.1:p.Val580Ile
NM_001136130.2:c.1963G>A	NP_001129602.1:p.Val655Ile
NM_001136131.2:c.1801G>A	NP_001129603.1:p.Val601Ile
NM_001204301.1:c.2077G>A	NP_001191230.1:p.Val693Ile
NM_001204302.1:c.2020G>A	NP_001191231.1:p.Val674Ile
NM_001204303.1:c.1852G>A	NP_001191232.1:p.Val618Ile
NM_201413.2:c.2074G>A	NP_958816.1:p.Val692Ile
NM_201414.2:c.1906G>A	NP_958817.1:p.Val636Ile
NM_000484.4:c.2131G>A MANE Select	NP_000475.1:p.Val711Ile
NM_001136129.3:c.1738G>A	NP_001129601.1:p.Val580Ile
NM_001136130.3:c.1963G>A	NP_001129602.1:p.Val655Ile
NM_001204301.2:c.2077G>A	NP_001191230.1:p.Val693Ile
NM_001204302.2:c.2020G>A	NP_001191231.1:p.Val674Ile
NM_001204303.2:c.1852G>A	NP_001191232.1:p.Val618Ile
NM_201413.3:c.2074G>A	NP_958816.1:p.Val692Ile
NM_201414.3:c.1906G>A	NP_958817.1:p.Val636Ile
NM_001136131.3:c.1801G>A	NP_001129603.1:p.Val601Ile
NM_001385253.1:c.1963G>A	NP_001372182.1:p.Val655Ile