Canonical Allele Identifier: CA409806270

Gene: APP

Linked Data

• dbSNP Id: rs1424019513
• MyVariant Identifiers: chr21:g.27269898T>A (hg19) ; chr21:g.25897586T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897586T>A , CM000683.2:g.25897586T>A	GRCh38
NC_000021.8:g.27269898T>A , CM000683.1:g.27269898T>A	GRCh37
NC_000021.7:g.26191769T>A	NCBI36
NG_007376.1:g.278235A>T
NG_007376.2:g.278543A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2018A>T
ENST00000707133.1:n.448A>T
ENST00000707134.1:n.717A>T
ENST00000346798.8:c.2051A>T MANE Select	ENSP00000284981.4:p.His684Leu
ENST00000346798.7:c.2051A>T	ENSP00000284981.4:p.His684Leu
ENST00000348990.9:c.1826A>T	ENSP00000345463.5:p.His609Leu
ENST00000354192.7:c.1658A>T	ENSP00000346129.3:p.His553Leu
ENST00000357903.7:c.1994A>T	ENSP00000350578.3:p.His665Leu
ENST00000358918.7:c.1997A>T	ENSP00000351796.3:p.His666Leu
ENST00000359726.7:c.1721A>T	ENSP00000352760.4:p.His574Leu
ENST00000439274.6:c.1883A>T	ENSP00000398879.2:p.His628Leu
ENST00000440126.7:c.1979A>T	ENSP00000387483.2:p.His660Leu
ENST00000464867.1:n.398A>T
NM_000484.3:c.2051A>T	NP_000475.1:p.His684Leu
NM_001136016.3:c.1979A>T	NP_001129488.1:p.His660Leu
NM_001136129.2:c.1658A>T	NP_001129601.1:p.His553Leu
NM_001136130.2:c.1883A>T	NP_001129602.1:p.His628Leu
NM_001136131.2:c.1721A>T	NP_001129603.1:p.His574Leu
NM_001204301.1:c.1997A>T	NP_001191230.1:p.His666Leu
NM_001204302.1:c.1940A>T	NP_001191231.1:p.His647Leu
NM_001204303.1:c.1772A>T	NP_001191232.1:p.His591Leu
NM_201413.2:c.1994A>T	NP_958816.1:p.His665Leu
NM_201414.2:c.1826A>T	NP_958817.1:p.His609Leu
NM_000484.4:c.2051A>T MANE Select	NP_000475.1:p.His684Leu
NM_001136129.3:c.1658A>T	NP_001129601.1:p.His553Leu
NM_001136130.3:c.1883A>T	NP_001129602.1:p.His628Leu
NM_001204301.2:c.1997A>T	NP_001191230.1:p.His666Leu
NM_001204302.2:c.1940A>T	NP_001191231.1:p.His647Leu
NM_001204303.2:c.1772A>T	NP_001191232.1:p.His591Leu
NM_201413.3:c.1994A>T	NP_958816.1:p.His665Leu
NM_201414.3:c.1826A>T	NP_958817.1:p.His609Leu
NM_001136131.3:c.1721A>T	NP_001129603.1:p.His574Leu
NM_001385253.1:c.1883A>T	NP_001372182.1:p.His628Leu