Canonical Allele Identifier: CA409806529
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897645C>G , CM000683.2:g.25897645C>G GRCh38
NC_000021.8:g.27269957C>G , CM000683.1:g.27269957C>G GRCh37
NC_000021.7:g.26191828C>G NCBI36
NG_007376.1:g.278176G>C
NG_007376.2:g.278484G>C

Transcript Alleles

HGVS Amino-acid change
NM_000484.3:c.1992G>C NP_000475.1:p.Glu664Asp
NM_001136016.3:c.1920G>C NP_001129488.1:p.Glu640Asp
NM_001136129.2:c.1599G>C NP_001129601.1:p.Glu533Asp
NM_001136130.2:c.1824G>C NP_001129602.1:p.Glu608Asp
NM_001136131.2:c.1662G>C NP_001129603.1:p.Glu554Asp
NM_001204301.1:c.1938G>C NP_001191230.1:p.Glu646Asp
NM_001204302.1:c.1881G>C NP_001191231.1:p.Glu627Asp
NM_001204303.1:c.1713G>C NP_001191232.1:p.Glu571Asp
NM_201413.2:c.1935G>C NP_958816.1:p.Glu645Asp
NM_201414.2:c.1767G>C NP_958817.1:p.Glu589Asp
NM_000484.4:c.1992G>C MANE Select NP_000475.1:p.Glu664Asp
NM_001136129.3:c.1599G>C NP_001129601.1:p.Glu533Asp
NM_001136130.3:c.1824G>C NP_001129602.1:p.Glu608Asp
NM_001204301.2:c.1938G>C NP_001191230.1:p.Glu646Asp
NM_001204302.2:c.1881G>C NP_001191231.1:p.Glu627Asp
NM_001204303.2:c.1713G>C NP_001191232.1:p.Glu571Asp
NM_201413.3:c.1935G>C NP_958816.1:p.Glu645Asp
NM_201414.3:c.1767G>C NP_958817.1:p.Glu589Asp
NM_001136131.3:c.1662G>C NP_001129603.1:p.Glu554Asp
NM_001385253.1:c.1824G>C NP_001372182.1:p.Glu608Asp
ENST00000346798.7:c.1992G>C ENSP00000284981.4:p.Glu664Asp
ENST00000348990.9:c.1767G>C ENSP00000345463.5:p.Glu589Asp
ENST00000354192.7:c.1599G>C ENSP00000346129.3:p.Glu533Asp
ENST00000357903.7:c.1935G>C ENSP00000350578.3:p.Glu645Asp
ENST00000358918.7:c.1938G>C ENSP00000351796.3:p.Glu646Asp
ENST00000359726.7:c.1662G>C ENSP00000352760.4:p.Glu554Asp
ENST00000439274.6:c.1824G>C ENSP00000398879.2:p.Glu608Asp
ENST00000440126.7:c.1920G>C ENSP00000387483.2:p.Glu640Asp
ENST00000464867.1:n.339G>C