Canonical Allele Identifier: CA409806212
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897574A>G , CM000683.2:g.25897574A>G GRCh38
NC_000021.8:g.27269886A>G , CM000683.1:g.27269886A>G GRCh37
NC_000021.7:g.26191757A>G NCBI36
NG_007376.1:g.278247T>C
NG_007376.2:g.278555T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2030T>C
ENST00000707133.1:n.460T>C
ENST00000707134.1:n.729T>C
ENST00000346798.8:c.2063T>C MANE Select ENSP00000284981.4:p.Leu688Ser
ENST00000346798.7:c.2063T>C ENSP00000284981.4:p.Leu688Ser
ENST00000348990.9:c.1838T>C ENSP00000345463.5:p.Leu613Ser
ENST00000354192.7:c.1670T>C ENSP00000346129.3:p.Leu557Ser
ENST00000357903.7:c.2006T>C ENSP00000350578.3:p.Leu669Ser
ENST00000358918.7:c.2009T>C ENSP00000351796.3:p.Leu670Ser
ENST00000359726.7:c.1733T>C ENSP00000352760.4:p.Leu578Ser
ENST00000439274.6:c.1895T>C ENSP00000398879.2:p.Leu632Ser
ENST00000440126.7:c.1991T>C ENSP00000387483.2:p.Leu664Ser
ENST00000464867.1:n.410T>C
NM_000484.3:c.2063T>C NP_000475.1:p.Leu688Ser
NM_001136016.3:c.1991T>C NP_001129488.1:p.Leu664Ser
NM_001136129.2:c.1670T>C NP_001129601.1:p.Leu557Ser
NM_001136130.2:c.1895T>C NP_001129602.1:p.Leu632Ser
NM_001136131.2:c.1733T>C NP_001129603.1:p.Leu578Ser
NM_001204301.1:c.2009T>C NP_001191230.1:p.Leu670Ser
NM_001204302.1:c.1952T>C NP_001191231.1:p.Leu651Ser
NM_001204303.1:c.1784T>C NP_001191232.1:p.Leu595Ser
NM_201413.2:c.2006T>C NP_958816.1:p.Leu669Ser
NM_201414.2:c.1838T>C NP_958817.1:p.Leu613Ser
NM_000484.4:c.2063T>C MANE Select NP_000475.1:p.Leu688Ser
NM_001136129.3:c.1670T>C NP_001129601.1:p.Leu557Ser
NM_001136130.3:c.1895T>C NP_001129602.1:p.Leu632Ser
NM_001204301.2:c.2009T>C NP_001191230.1:p.Leu670Ser
NM_001204302.2:c.1952T>C NP_001191231.1:p.Leu651Ser
NM_001204303.2:c.1784T>C NP_001191232.1:p.Leu595Ser
NM_201413.3:c.2006T>C NP_958816.1:p.Leu669Ser
NM_201414.3:c.1838T>C NP_958817.1:p.Leu613Ser
NM_001136131.3:c.1733T>C NP_001129603.1:p.Leu578Ser
NM_001385253.1:c.1895T>C NP_001372182.1:p.Leu632Ser