Canonical Allele Identifier: CA409806579

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27269977A>T (hg19) ; chr21:g.25897665A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897665A>T , CM000683.2:g.25897665A>T	GRCh38
NC_000021.8:g.27269977A>T , CM000683.1:g.27269977A>T	GRCh37
NC_000021.7:g.26191848A>T	NCBI36
NG_007376.1:g.278156T>A
NG_007376.2:g.278464T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.1939T>A
ENST00000707133.1:n.369T>A
ENST00000707134.1:n.638T>A
ENST00000346798.8:c.1972T>A MANE Select	ENSP00000284981.4:p.Leu658Met
ENST00000346798.7:c.1972T>A	ENSP00000284981.4:p.Leu658Met
ENST00000348990.9:c.1747T>A	ENSP00000345463.5:p.Leu583Met
ENST00000354192.7:c.1579T>A	ENSP00000346129.3:p.Leu527Met
ENST00000357903.7:c.1915T>A	ENSP00000350578.3:p.Leu639Met
ENST00000358918.7:c.1918T>A	ENSP00000351796.3:p.Leu640Met
ENST00000359726.7:c.1642T>A	ENSP00000352760.4:p.Leu548Met
ENST00000439274.6:c.1804T>A	ENSP00000398879.2:p.Leu602Met
ENST00000440126.7:c.1900T>A	ENSP00000387483.2:p.Leu634Met
ENST00000464867.1:n.319T>A
NM_000484.3:c.1972T>A	NP_000475.1:p.Leu658Met
NM_001136016.3:c.1900T>A	NP_001129488.1:p.Leu634Met
NM_001136129.2:c.1579T>A	NP_001129601.1:p.Leu527Met
NM_001136130.2:c.1804T>A	NP_001129602.1:p.Leu602Met
NM_001136131.2:c.1642T>A	NP_001129603.1:p.Leu548Met
NM_001204301.1:c.1918T>A	NP_001191230.1:p.Leu640Met
NM_001204302.1:c.1861T>A	NP_001191231.1:p.Leu621Met
NM_001204303.1:c.1693T>A	NP_001191232.1:p.Leu565Met
NM_201413.2:c.1915T>A	NP_958816.1:p.Leu639Met
NM_201414.2:c.1747T>A	NP_958817.1:p.Leu583Met
NM_000484.4:c.1972T>A MANE Select	NP_000475.1:p.Leu658Met
NM_001136129.3:c.1579T>A	NP_001129601.1:p.Leu527Met
NM_001136130.3:c.1804T>A	NP_001129602.1:p.Leu602Met
NM_001204301.2:c.1918T>A	NP_001191230.1:p.Leu640Met
NM_001204302.2:c.1861T>A	NP_001191231.1:p.Leu621Met
NM_001204303.2:c.1693T>A	NP_001191232.1:p.Leu565Met
NM_201413.3:c.1915T>A	NP_958816.1:p.Leu639Met
NM_201414.3:c.1747T>A	NP_958817.1:p.Leu583Met
NM_001136131.3:c.1642T>A	NP_001129603.1:p.Leu548Met
NM_001385253.1:c.1804T>A	NP_001372182.1:p.Leu602Met