Canonical Allele Identifier: CA409805534
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891774A>G , CM000683.2:g.25891774A>G GRCh38
NC_000021.8:g.27264086A>G , CM000683.1:g.27264086A>G GRCh37
NC_000021.7:g.26185957A>G NCBI36
NG_007376.1:g.284047T>C
NG_007376.2:g.284355T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2159T>C MANE Select ENSP00000284981.4:p.Leu720Ser
ENST00000346798.7:c.2159T>C ENSP00000284981.4:p.Leu720Ser
ENST00000348990.9:c.1934T>C ENSP00000345463.5:p.Leu645Ser
ENST00000354192.7:c.1766T>C ENSP00000346129.3:p.Leu589Ser
ENST00000357903.7:c.2102T>C ENSP00000350578.3:p.Leu701Ser
ENST00000358918.7:c.2105T>C ENSP00000351796.3:p.Leu702Ser
ENST00000359726.7:c.1829T>C ENSP00000352760.4:p.Leu610Ser
ENST00000439274.6:c.1991T>C ENSP00000398879.2:p.Leu664Ser
ENST00000440126.7:c.2087T>C ENSP00000387483.2:p.Leu696Ser
ENST00000464867.1:n.506T>C
NM_000484.3:c.2159T>C NP_000475.1:p.Leu720Ser
NM_001136016.3:c.2087T>C NP_001129488.1:p.Leu696Ser
NM_001136129.2:c.1766T>C NP_001129601.1:p.Leu589Ser
NM_001136130.2:c.1991T>C NP_001129602.1:p.Leu664Ser
NM_001136131.2:c.1829T>C NP_001129603.1:p.Leu610Ser
NM_001204301.1:c.2105T>C NP_001191230.1:p.Leu702Ser
NM_001204302.1:c.2048T>C NP_001191231.1:p.Leu683Ser
NM_001204303.1:c.1880T>C NP_001191232.1:p.Leu627Ser
NM_201413.2:c.2102T>C NP_958816.1:p.Leu701Ser
NM_201414.2:c.1934T>C NP_958817.1:p.Leu645Ser
NM_000484.4:c.2159T>C MANE Select NP_000475.1:p.Leu720Ser
NM_001136129.3:c.1766T>C NP_001129601.1:p.Leu589Ser
NM_001136130.3:c.1991T>C NP_001129602.1:p.Leu664Ser
NM_001204301.2:c.2105T>C NP_001191230.1:p.Leu702Ser
NM_001204302.2:c.2048T>C NP_001191231.1:p.Leu683Ser
NM_001204303.2:c.1880T>C NP_001191232.1:p.Leu627Ser
NM_201413.3:c.2102T>C NP_958816.1:p.Leu701Ser
NM_201414.3:c.1934T>C NP_958817.1:p.Leu645Ser
NM_001136131.3:c.1829T>C NP_001129603.1:p.Leu610Ser
NM_001385253.1:c.1991T>C NP_001372182.1:p.Leu664Ser