Canonical Allele Identifier: CA2654123650
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897799_25897806del , CM000683.2:g.25897799_25897806del GRCh38
NC_000021.8:g.27270111_27270118del , CM000683.1:g.27270111_27270118del GRCh37
NC_000021.7:g.26191982_26191989del NCBI36
NG_007376.1:g.278015_278022del
NG_007376.2:g.278323_278330del

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.1931-133_1931-126del
ENST00000707133.1:n.361-133_361-126del
ENST00000707134.1:n.630-133_630-126del
ENST00000346798.8:c.1964-133_1964-126del MANE Select ENSP00000284981.4:n.1964-133_1964-126del
ENST00000346798.7:c.1964-133_1964-126del ENSP00000284981.4:n.1964-133_1964-126del
ENST00000348990.9:c.1739-133_1739-126del ENSP00000345463.5:n.1739-133_1739-126del
ENST00000354192.7:c.1571-133_1571-126del ENSP00000346129.3:n.1571-133_1571-126del
ENST00000357903.7:c.1907-133_1907-126del ENSP00000350578.3:n.1907-133_1907-126del
ENST00000358918.7:c.1910-133_1910-126del ENSP00000351796.3:n.1910-133_1910-126del
ENST00000359726.7:c.1634-133_1634-126del ENSP00000352760.4:n.1634-133_1634-126del
ENST00000439274.6:c.1796-133_1796-126del ENSP00000398879.2:n.1796-133_1796-126del
ENST00000440126.7:c.1892-133_1892-126del ENSP00000387483.2:n.1892-133_1892-126del
ENST00000464867.1:n.178_185del
NM_000484.3:c.1964-133_1964-126del NP_000475.1:n.1964-133_1964-126del
NM_001136016.3:c.1892-133_1892-126del NP_001129488.1:n.1892-133_1892-126del
NM_001136129.2:c.1571-133_1571-126del NP_001129601.1:n.1571-133_1571-126del
NM_001136130.2:c.1796-133_1796-126del NP_001129602.1:n.1796-133_1796-126del
NM_001136131.2:c.1634-133_1634-126del NP_001129603.1:n.1634-133_1634-126del
NM_001204301.1:c.1910-133_1910-126del NP_001191230.1:n.1910-133_1910-126del
NM_001204302.1:c.1853-133_1853-126del NP_001191231.1:n.1853-133_1853-126del
NM_001204303.1:c.1685-133_1685-126del NP_001191232.1:n.1685-133_1685-126del
NM_201413.2:c.1907-133_1907-126del NP_958816.1:n.1907-133_1907-126del
NM_201414.2:c.1739-133_1739-126del NP_958817.1:n.1739-133_1739-126del
NM_000484.4:c.1964-133_1964-126del MANE Select NP_000475.1:n.1964-133_1964-126del
NM_001136129.3:c.1571-133_1571-126del NP_001129601.1:n.1571-133_1571-126del
NM_001136130.3:c.1796-133_1796-126del NP_001129602.1:n.1796-133_1796-126del
NM_001204301.2:c.1910-133_1910-126del NP_001191230.1:n.1910-133_1910-126del
NM_001204302.2:c.1853-133_1853-126del NP_001191231.1:n.1853-133_1853-126del
NM_001204303.2:c.1685-133_1685-126del NP_001191232.1:n.1685-133_1685-126del
NM_201413.3:c.1907-133_1907-126del NP_958816.1:n.1907-133_1907-126del
NM_201414.3:c.1739-133_1739-126del NP_958817.1:n.1739-133_1739-126del
NM_001136131.3:c.1634-133_1634-126del NP_001129603.1:n.1634-133_1634-126del
NM_001385253.1:c.1796-133_1796-126del NP_001372182.1:n.1796-133_1796-126del