Canonical Allele Identifier: CA511686029
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs1239570473

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891830T>G , CM000683.2:g.25891830T>G GRCh38
NC_000021.8:g.27264142T>G , CM000683.1:g.27264142T>G GRCh37
NC_000021.7:g.26186013T>G NCBI36
NG_007376.1:g.283991A>C
NG_007376.2:g.284299A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2070A>C
ENST00000707133.1:n.500A>C
ENST00000707134.1:n.769A>C
ENST00000346798.8:c.2103A>C MANE Select ENSP00000284981.4:p.Ala701=
ENST00000346798.7:c.2103A>C ENSP00000284981.4:p.Ala701=
ENST00000348990.9:c.1878A>C ENSP00000345463.5:p.Ala626=
ENST00000354192.7:c.1710A>C ENSP00000346129.3:p.Ala570=
ENST00000357903.7:c.2046A>C ENSP00000350578.3:p.Ala682=
ENST00000358918.7:c.2049A>C ENSP00000351796.3:p.Ala683=
ENST00000359726.7:c.1773A>C ENSP00000352760.4:p.Ala591=
ENST00000439274.6:c.1935A>C ENSP00000398879.2:p.Ala645=
ENST00000440126.7:c.2031A>C ENSP00000387483.2:p.Ala677=
ENST00000464867.1:n.450A>C
NM_000484.3:c.2103A>C NP_000475.1:p.Ala701=
NM_001136016.3:c.2031A>C NP_001129488.1:p.Ala677=
NM_001136129.2:c.1710A>C NP_001129601.1:p.Ala570=
NM_001136130.2:c.1935A>C NP_001129602.1:p.Ala645=
NM_001136131.2:c.1773A>C NP_001129603.1:p.Ala591=
NM_001204301.1:c.2049A>C NP_001191230.1:p.Ala683=
NM_001204302.1:c.1992A>C NP_001191231.1:p.Ala664=
NM_001204303.1:c.1824A>C NP_001191232.1:p.Ala608=
NM_201413.2:c.2046A>C NP_958816.1:p.Ala682=
NM_201414.2:c.1878A>C NP_958817.1:p.Ala626=
NM_000484.4:c.2103A>C MANE Select NP_000475.1:p.Ala701=
NM_001136129.3:c.1710A>C NP_001129601.1:p.Ala570=
NM_001136130.3:c.1935A>C NP_001129602.1:p.Ala645=
NM_001204301.2:c.2049A>C NP_001191230.1:p.Ala683=
NM_001204302.2:c.1992A>C NP_001191231.1:p.Ala664=
NM_001204303.2:c.1824A>C NP_001191232.1:p.Ala608=
NM_201413.3:c.2046A>C NP_958816.1:p.Ala682=
NM_201414.3:c.1878A>C NP_958817.1:p.Ala626=
NM_001136131.3:c.1773A>C NP_001129603.1:p.Ala591=
NM_001385253.1:c.1935A>C NP_001372182.1:p.Ala645=