Canonical Allele Identifier: CA3243796646

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891768A= , CM000683.2:g.25891768A=	GRCh38
NC_000021.8:g.27264080A= , CM000683.1:g.27264080A=	GRCh37
NC_000021.7:g.26185951A=	NCBI36
NG_007376.1:g.284053T=
NG_007376.2:g.284361T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000484.4:c.2165T= MANE Select	NP_000475.1:p.Met722=
ENST00000346798.8:c.2165T= MANE Select	ENSP00000284981.4:p.Met722=
NM_000484.3:c.2165T=	NP_000475.1:p.Met722=
NM_001136016.3:c.2093T=	NP_001129488.1:p.Met698=
NM_001136129.2:c.1772T=	NP_001129601.1:p.Met591=
NM_001136129.3:c.1772T=	NP_001129601.1:p.Met591=
NM_001136130.2:c.1997T=	NP_001129602.1:p.Met666=
NM_001136130.3:c.1997T=	NP_001129602.1:p.Met666=
NM_001136131.2:c.1835T=	NP_001129603.1:p.Met612=
NM_001136131.3:c.1835T=	NP_001129603.1:p.Met612=
NM_001204301.1:c.2111T=	NP_001191230.1:p.Met704=
NM_001204301.2:c.2111T=	NP_001191230.1:p.Met704=
NM_001204302.1:c.2054T=	NP_001191231.1:p.Met685=
NM_001204302.2:c.2054T=	NP_001191231.1:p.Met685=
NM_001204303.1:c.1886T=	NP_001191232.1:p.Met629=
NM_001204303.2:c.1886T=	NP_001191232.1:p.Met629=
NM_001385253.1:c.1997T=	NP_001372182.1:p.Met666=
NM_201413.2:c.2108T=	NP_958816.1:p.Met703=
NM_201413.3:c.2108T=	NP_958816.1:p.Met703=
NM_201414.2:c.1940T=	NP_958817.1:p.Met647=
NM_201414.3:c.1940T=	NP_958817.1:p.Met647=
ENST00000346798.7:c.2165T=	ENSP00000284981.4:p.Met722=
ENST00000348990.9:c.1940T=	ENSP00000345463.5:p.Met647=
ENST00000354192.7:c.1772T=	ENSP00000346129.3:p.Met591=
ENST00000357903.7:c.2108T=	ENSP00000350578.3:p.Met703=
ENST00000358918.7:c.2111T=	ENSP00000351796.3:p.Met704=
ENST00000359726.7:c.1835T=	ENSP00000352760.4:p.Met612=
ENST00000439274.6:c.1997T=	ENSP00000398879.2:p.Met666=
ENST00000440126.7:c.2093T=	ENSP00000387483.2:p.Met698=
ENST00000464867.1:n.512T=
ENST00000707132.1:n.2132T=
ENST00000707133.1:n.562T=
ENST00000707134.1:n.831T=