Canonical Allele Identifier: CA409805461

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891744G>T , CM000683.2:g.25891744G>T	GRCh38
NC_000021.8:g.27264056G>T , CM000683.1:g.27264056G>T	GRCh37
NC_000021.7:g.26185927G>T	NCBI36
NG_007376.1:g.284077C>A
NG_007376.2:g.284385C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000484.4:c.2189C>A MANE Select	NP_000475.1:p.Ser730Tyr
ENST00000346798.8:c.2189C>A MANE Select	ENSP00000284981.4:p.Ser730Tyr
NM_000484.3:c.2189C>A	NP_000475.1:p.Ser730Tyr
NM_001136016.3:c.2117C>A	NP_001129488.1:p.Ser706Tyr
NM_001136129.2:c.1796C>A	NP_001129601.1:p.Ser599Tyr
NM_001136129.3:c.1796C>A	NP_001129601.1:p.Ser599Tyr
NM_001136130.2:c.2021C>A	NP_001129602.1:p.Ser674Tyr
NM_001136130.3:c.2021C>A	NP_001129602.1:p.Ser674Tyr
NM_001136131.2:c.1859C>A	NP_001129603.1:p.Ser620Tyr
NM_001136131.3:c.1859C>A	NP_001129603.1:p.Ser620Tyr
NM_001204301.1:c.2135C>A	NP_001191230.1:p.Ser712Tyr
NM_001204301.2:c.2135C>A	NP_001191230.1:p.Ser712Tyr
NM_001204302.1:c.2078C>A	NP_001191231.1:p.Ser693Tyr
NM_001204302.2:c.2078C>A	NP_001191231.1:p.Ser693Tyr
NM_001204303.1:c.1910C>A	NP_001191232.1:p.Ser637Tyr
NM_001204303.2:c.1910C>A	NP_001191232.1:p.Ser637Tyr
NM_001385253.1:c.2021C>A	NP_001372182.1:p.Ser674Tyr
NM_201413.2:c.2132C>A	NP_958816.1:p.Ser711Tyr
NM_201413.3:c.2132C>A	NP_958816.1:p.Ser711Tyr
NM_201414.2:c.1964C>A	NP_958817.1:p.Ser655Tyr
NM_201414.3:c.1964C>A	NP_958817.1:p.Ser655Tyr
ENST00000346798.7:c.2189C>A	ENSP00000284981.4:p.Ser730Tyr
ENST00000348990.9:c.1964C>A	ENSP00000345463.5:p.Ser655Tyr
ENST00000354192.7:c.1796C>A	ENSP00000346129.3:p.Ser599Tyr
ENST00000357903.7:c.2132C>A	ENSP00000350578.3:p.Ser711Tyr
ENST00000358918.7:c.2135C>A	ENSP00000351796.3:p.Ser712Tyr
ENST00000359726.7:c.1859C>A	ENSP00000352760.4:p.Ser620Tyr
ENST00000439274.6:c.2021C>A	ENSP00000398879.2:p.Ser674Tyr
ENST00000440126.7:c.2117C>A	ENSP00000387483.2:p.Ser706Tyr
ENST00000464867.1:n.536C>A
ENST00000707132.1:n.2156C>A
ENST00000707133.1:n.586C>A
ENST00000707134.1:n.855C>A