Canonical Allele Identifier: CA409806370

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27269920G>T (hg19) ; chr21:g.25897608G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897608G>T , CM000683.2:g.25897608G>T	GRCh38
NC_000021.8:g.27269920G>T , CM000683.1:g.27269920G>T	GRCh37
NC_000021.7:g.26191791G>T	NCBI36
NG_007376.1:g.278213C>A
NG_007376.2:g.278521C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1996C>A
ENST00000707133.1:n.426C>A
ENST00000707134.1:n.695C>A
ENST00000346798.8:c.2029C>A MANE Select	ENSP00000284981.4:p.His677Asn
ENST00000346798.7:c.2029C>A	ENSP00000284981.4:p.His677Asn
ENST00000348990.9:c.1804C>A	ENSP00000345463.5:p.His602Asn
ENST00000354192.7:c.1636C>A	ENSP00000346129.3:p.His546Asn
ENST00000357903.7:c.1972C>A	ENSP00000350578.3:p.His658Asn
ENST00000358918.7:c.1975C>A	ENSP00000351796.3:p.His659Asn
ENST00000359726.7:c.1699C>A	ENSP00000352760.4:p.His567Asn
ENST00000439274.6:c.1861C>A	ENSP00000398879.2:p.His621Asn
ENST00000440126.7:c.1957C>A	ENSP00000387483.2:p.His653Asn
ENST00000464867.1:n.376C>A
NM_000484.3:c.2029C>A	NP_000475.1:p.His677Asn
NM_001136016.3:c.1957C>A	NP_001129488.1:p.His653Asn
NM_001136129.2:c.1636C>A	NP_001129601.1:p.His546Asn
NM_001136130.2:c.1861C>A	NP_001129602.1:p.His621Asn
NM_001136131.2:c.1699C>A	NP_001129603.1:p.His567Asn
NM_001204301.1:c.1975C>A	NP_001191230.1:p.His659Asn
NM_001204302.1:c.1918C>A	NP_001191231.1:p.His640Asn
NM_001204303.1:c.1750C>A	NP_001191232.1:p.His584Asn
NM_201413.2:c.1972C>A	NP_958816.1:p.His658Asn
NM_201414.2:c.1804C>A	NP_958817.1:p.His602Asn
NM_000484.4:c.2029C>A MANE Select	NP_000475.1:p.His677Asn
NM_001136129.3:c.1636C>A	NP_001129601.1:p.His546Asn
NM_001136130.3:c.1861C>A	NP_001129602.1:p.His621Asn
NM_001204301.2:c.1975C>A	NP_001191230.1:p.His659Asn
NM_001204302.2:c.1918C>A	NP_001191231.1:p.His640Asn
NM_001204303.2:c.1750C>A	NP_001191232.1:p.His584Asn
NM_201413.3:c.1972C>A	NP_958816.1:p.His658Asn
NM_201414.3:c.1804C>A	NP_958817.1:p.His602Asn
NM_001136131.3:c.1699C>A	NP_001129603.1:p.His567Asn
NM_001385253.1:c.1861C>A	NP_001372182.1:p.His621Asn