Canonical Allele Identifier: CA1021421475
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs2037707603

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891680_25891681del , CM000683.2:g.25891680_25891681del GRCh38
NC_000021.8:g.27263992_27263993del , CM000683.1:g.27263992_27263993del GRCh37
NC_000021.7:g.26185863_26185864del NCBI36
NG_007376.1:g.284140_284141del
NG_007376.2:g.284448_284449del

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2211+41_2211+42del MANE Select ENSP00000284981.4:p.=
ENST00000346798.7:c.2211+41_2211+42del ENSP00000284981.4:p.=
ENST00000348990.9:c.1986+41_1986+42del ENSP00000345463.5:p.=
ENST00000354192.7:c.1818+41_1818+42del ENSP00000346129.3:p.=
ENST00000357903.7:c.2154+41_2154+42del ENSP00000350578.3:p.=
ENST00000358918.7:c.2157+41_2157+42del ENSP00000351796.3:p.=
ENST00000359726.7:c.1881+41_1881+42del ENSP00000352760.4:p.=
ENST00000439274.6:c.2043+41_2043+42del ENSP00000398879.2:p.=
ENST00000440126.7:c.2139+41_2139+42del ENSP00000387483.2:p.=
ENST00000464867.1:n.558+41_558+42del
NM_000484.3:c.2211+41_2211+42del NP_000475.1:p.=
NM_001136016.3:c.2139+41_2139+42del NP_001129488.1:p.=
NM_001136129.2:c.1818+41_1818+42del NP_001129601.1:p.=
NM_001136130.2:c.2043+41_2043+42del NP_001129602.1:p.=
NM_001136131.2:c.1881+41_1881+42del NP_001129603.1:p.=
NM_001204301.1:c.2157+41_2157+42del NP_001191230.1:p.=
NM_001204302.1:c.2100+41_2100+42del NP_001191231.1:p.=
NM_001204303.1:c.1932+41_1932+42del NP_001191232.1:p.=
NM_201413.2:c.2154+41_2154+42del NP_958816.1:p.=
NM_201414.2:c.1986+41_1986+42del NP_958817.1:p.=
NM_000484.4:c.2211+41_2211+42del MANE Select NP_000475.1:p.=
NM_001136129.3:c.1818+41_1818+42del NP_001129601.1:p.=
NM_001136130.3:c.2043+41_2043+42del NP_001129602.1:p.=
NM_001204301.2:c.2157+41_2157+42del NP_001191230.1:p.=
NM_001204302.2:c.2100+41_2100+42del NP_001191231.1:p.=
NM_001204303.2:c.1932+41_1932+42del NP_001191232.1:p.=
NM_201413.3:c.2154+41_2154+42del NP_958816.1:p.=
NM_201414.3:c.1986+41_1986+42del NP_958817.1:p.=
NM_001136131.3:c.1881+41_1881+42del NP_001129603.1:p.=
NM_001385253.1:c.2043+41_2043+42del NP_001372182.1:p.=