Canonical Allele Identifier: CA409806261

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27269896G>A (hg19) ; chr21:g.25897584G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897584G>A , CM000683.2:g.25897584G>A	GRCh38
NC_000021.8:g.27269896G>A , CM000683.1:g.27269896G>A	GRCh37
NC_000021.7:g.26191767G>A	NCBI36
NG_007376.1:g.278237C>T
NG_007376.2:g.278545C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2020C>T
ENST00000707133.1:n.450C>T
ENST00000707134.1:n.719C>T
ENST00000346798.8:c.2053C>T MANE Select	ENSP00000284981.4:p.His685Tyr
ENST00000346798.7:c.2053C>T	ENSP00000284981.4:p.His685Tyr
ENST00000348990.9:c.1828C>T	ENSP00000345463.5:p.His610Tyr
ENST00000354192.7:c.1660C>T	ENSP00000346129.3:p.His554Tyr
ENST00000357903.7:c.1996C>T	ENSP00000350578.3:p.His666Tyr
ENST00000358918.7:c.1999C>T	ENSP00000351796.3:p.His667Tyr
ENST00000359726.7:c.1723C>T	ENSP00000352760.4:p.His575Tyr
ENST00000439274.6:c.1885C>T	ENSP00000398879.2:p.His629Tyr
ENST00000440126.7:c.1981C>T	ENSP00000387483.2:p.His661Tyr
ENST00000464867.1:n.400C>T
NM_000484.3:c.2053C>T	NP_000475.1:p.His685Tyr
NM_001136016.3:c.1981C>T	NP_001129488.1:p.His661Tyr
NM_001136129.2:c.1660C>T	NP_001129601.1:p.His554Tyr
NM_001136130.2:c.1885C>T	NP_001129602.1:p.His629Tyr
NM_001136131.2:c.1723C>T	NP_001129603.1:p.His575Tyr
NM_001204301.1:c.1999C>T	NP_001191230.1:p.His667Tyr
NM_001204302.1:c.1942C>T	NP_001191231.1:p.His648Tyr
NM_001204303.1:c.1774C>T	NP_001191232.1:p.His592Tyr
NM_201413.2:c.1996C>T	NP_958816.1:p.His666Tyr
NM_201414.2:c.1828C>T	NP_958817.1:p.His610Tyr
NM_000484.4:c.2053C>T MANE Select	NP_000475.1:p.His685Tyr
NM_001136129.3:c.1660C>T	NP_001129601.1:p.His554Tyr
NM_001136130.3:c.1885C>T	NP_001129602.1:p.His629Tyr
NM_001204301.2:c.1999C>T	NP_001191230.1:p.His667Tyr
NM_001204302.2:c.1942C>T	NP_001191231.1:p.His648Tyr
NM_001204303.2:c.1774C>T	NP_001191232.1:p.His592Tyr
NM_201413.3:c.1996C>T	NP_958816.1:p.His666Tyr
NM_201414.3:c.1828C>T	NP_958817.1:p.His610Tyr
NM_001136131.3:c.1723C>T	NP_001129603.1:p.His575Tyr
NM_001385253.1:c.1885C>T	NP_001372182.1:p.His629Tyr