Canonical Allele Identifier: CA409806380
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897612G>C , CM000683.2:g.25897612G>C GRCh38
NC_000021.8:g.27269924G>C , CM000683.1:g.27269924G>C GRCh37
NC_000021.7:g.26191795G>C NCBI36
NG_007376.1:g.278209C>G
NG_007376.2:g.278517C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.1992C>G
ENST00000707133.1:n.422C>G
ENST00000707134.1:n.691C>G
ENST00000346798.8:c.2025C>G MANE Select ENSP00000284981.4:p.Phe675Leu
ENST00000346798.7:c.2025C>G ENSP00000284981.4:p.Phe675Leu
ENST00000348990.9:c.1800C>G ENSP00000345463.5:p.Phe600Leu
ENST00000354192.7:c.1632C>G ENSP00000346129.3:p.Phe544Leu
ENST00000357903.7:c.1968C>G ENSP00000350578.3:p.Phe656Leu
ENST00000358918.7:c.1971C>G ENSP00000351796.3:p.Phe657Leu
ENST00000359726.7:c.1695C>G ENSP00000352760.4:p.Phe565Leu
ENST00000439274.6:c.1857C>G ENSP00000398879.2:p.Phe619Leu
ENST00000440126.7:c.1953C>G ENSP00000387483.2:p.Phe651Leu
ENST00000464867.1:n.372C>G
NM_000484.3:c.2025C>G NP_000475.1:p.Phe675Leu
NM_001136016.3:c.1953C>G NP_001129488.1:p.Phe651Leu
NM_001136129.2:c.1632C>G NP_001129601.1:p.Phe544Leu
NM_001136130.2:c.1857C>G NP_001129602.1:p.Phe619Leu
NM_001136131.2:c.1695C>G NP_001129603.1:p.Phe565Leu
NM_001204301.1:c.1971C>G NP_001191230.1:p.Phe657Leu
NM_001204302.1:c.1914C>G NP_001191231.1:p.Phe638Leu
NM_001204303.1:c.1746C>G NP_001191232.1:p.Phe582Leu
NM_201413.2:c.1968C>G NP_958816.1:p.Phe656Leu
NM_201414.2:c.1800C>G NP_958817.1:p.Phe600Leu
NM_000484.4:c.2025C>G MANE Select NP_000475.1:p.Phe675Leu
NM_001136129.3:c.1632C>G NP_001129601.1:p.Phe544Leu
NM_001136130.3:c.1857C>G NP_001129602.1:p.Phe619Leu
NM_001204301.2:c.1971C>G NP_001191230.1:p.Phe657Leu
NM_001204302.2:c.1914C>G NP_001191231.1:p.Phe638Leu
NM_001204303.2:c.1746C>G NP_001191232.1:p.Phe582Leu
NM_201413.3:c.1968C>G NP_958816.1:p.Phe656Leu
NM_201414.3:c.1800C>G NP_958817.1:p.Phe600Leu
NM_001136131.3:c.1695C>G NP_001129603.1:p.Phe565Leu
NM_001385253.1:c.1857C>G NP_001372182.1:p.Phe619Leu