Canonical Allele Identifier: CA2383551548

Gene: APP

Linked Data

• dbSNP Id: rs2037702831

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891641_25891642insGC , CM000683.2:g.25891641_25891642insGC	GRCh38
NC_000021.8:g.27263953_27263954insGC , CM000683.1:g.27263953_27263954insGC	GRCh37
NC_000021.7:g.26185824_26185825insGC	NCBI36
NG_007376.1:g.284179_284180insGC
NG_007376.2:g.284487_284488insGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2178+80_2178+81insGC
ENST00000707133.1:n.608+80_608+81insGC
ENST00000707134.1:n.877+80_877+81insGC
ENST00000346798.8:c.2211+80_2211+81insGC MANE Select	ENSP00000284981.4:n.2211+80_2211+81insGC
ENST00000346798.7:c.2211+80_2211+81insGC	ENSP00000284981.4:n.2211+80_2211+81insGC
ENST00000348990.9:c.1986+80_1986+81insGC	ENSP00000345463.5:n.1986+80_1986+81insGC
ENST00000354192.7:c.1818+80_1818+81insGC	ENSP00000346129.3:n.1818+80_1818+81insGC
ENST00000357903.7:c.2154+80_2154+81insGC	ENSP00000350578.3:n.2154+80_2154+81insGC
ENST00000358918.7:c.2157+80_2157+81insGC	ENSP00000351796.3:n.2157+80_2157+81insGC
ENST00000359726.7:c.1881+80_1881+81insGC	ENSP00000352760.4:n.1881+80_1881+81insGC
ENST00000439274.6:c.2043+80_2043+81insGC	ENSP00000398879.2:n.2043+80_2043+81insGC
ENST00000440126.7:c.2139+80_2139+81insGC	ENSP00000387483.2:n.2139+80_2139+81insGC
ENST00000464867.1:n.558+80_558+81insGC
NM_000484.3:c.2211+80_2211+81insGC	NP_000475.1:n.2211+80_2211+81insGC
NM_001136016.3:c.2139+80_2139+81insGC	NP_001129488.1:n.2139+80_2139+81insGC
NM_001136129.2:c.1818+80_1818+81insGC	NP_001129601.1:n.1818+80_1818+81insGC
NM_001136130.2:c.2043+80_2043+81insGC	NP_001129602.1:n.2043+80_2043+81insGC
NM_001136131.2:c.1881+80_1881+81insGC	NP_001129603.1:n.1881+80_1881+81insGC
NM_001204301.1:c.2157+80_2157+81insGC	NP_001191230.1:n.2157+80_2157+81insGC
NM_001204302.1:c.2100+80_2100+81insGC	NP_001191231.1:n.2100+80_2100+81insGC
NM_001204303.1:c.1932+80_1932+81insGC	NP_001191232.1:n.1932+80_1932+81insGC
NM_201413.2:c.2154+80_2154+81insGC	NP_958816.1:n.2154+80_2154+81insGC
NM_201414.2:c.1986+80_1986+81insGC	NP_958817.1:n.1986+80_1986+81insGC
NM_000484.4:c.2211+80_2211+81insGC MANE Select	NP_000475.1:n.2211+80_2211+81insGC
NM_001136129.3:c.1818+80_1818+81insGC	NP_001129601.1:n.1818+80_1818+81insGC
NM_001136130.3:c.2043+80_2043+81insGC	NP_001129602.1:n.2043+80_2043+81insGC
NM_001204301.2:c.2157+80_2157+81insGC	NP_001191230.1:n.2157+80_2157+81insGC
NM_001204302.2:c.2100+80_2100+81insGC	NP_001191231.1:n.2100+80_2100+81insGC
NM_001204303.2:c.1932+80_1932+81insGC	NP_001191232.1:n.1932+80_1932+81insGC
NM_201413.3:c.2154+80_2154+81insGC	NP_958816.1:n.2154+80_2154+81insGC
NM_201414.3:c.1986+80_1986+81insGC	NP_958817.1:n.1986+80_1986+81insGC
NM_001136131.3:c.1881+80_1881+81insGC	NP_001129603.1:n.1881+80_1881+81insGC
NM_001385253.1:c.2043+80_2043+81insGC	NP_001372182.1:n.2043+80_2043+81insGC