Canonical Allele Identifier: CA2383551395

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891305_25891310delinsCAAAAG , CM000683.2:g.25891305_25891310delinsCAAAAG	GRCh38
NC_000021.8:g.27263617_27263622delinsCAAAAG , CM000683.1:g.27263617_27263622delinsCAAAAG	GRCh37
NC_000021.7:g.26185488_26185493delinsCAAAAG	NCBI36
NG_007376.1:g.284511_284516delinsCTTTTG
NG_007376.2:g.284819_284824delinsCTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2178+412_2178+417delinsCTTTTG
ENST00000707133.1:n.608+412_608+417delinsCTTTTG
ENST00000707134.1:n.877+412_877+417delinsCTTTTG
ENST00000346798.8:c.2211+412_2211+417delinsCTTTTG MANE Select	ENSP00000284981.4:n.2211+412_2211+417delinsCTTTTG
ENST00000346798.7:c.2211+412_2211+417delinsCTTTTG	ENSP00000284981.4:n.2211+412_2211+417delinsCTTTTG
ENST00000348990.9:c.1986+412_1986+417delinsCTTTTG	ENSP00000345463.5:n.1986+412_1986+417delinsCTTTTG
ENST00000354192.7:c.1818+412_1818+417delinsCTTTTG	ENSP00000346129.3:n.1818+412_1818+417delinsCTTTTG
ENST00000357903.7:c.2154+412_2154+417delinsCTTTTG	ENSP00000350578.3:n.2154+412_2154+417delinsCTTTTG
ENST00000358918.7:c.2157+412_2157+417delinsCTTTTG	ENSP00000351796.3:n.2157+412_2157+417delinsCTTTTG
ENST00000359726.7:c.1881+412_1881+417delinsCTTTTG	ENSP00000352760.4:n.1881+412_1881+417delinsCTTTTG
ENST00000439274.6:c.2043+412_2043+417delinsCTTTTG	ENSP00000398879.2:n.2043+412_2043+417delinsCTTTTG
ENST00000440126.7:c.2139+412_2139+417delinsCTTTTG	ENSP00000387483.2:n.2139+412_2139+417delinsCTTTTG
ENST00000464867.1:n.558+412_558+417delinsCTTTTG
NM_000484.3:c.2211+412_2211+417delinsCTTTTG	NP_000475.1:n.2211+412_2211+417delinsCTTTTG
NM_001136016.3:c.2139+412_2139+417delinsCTTTTG	NP_001129488.1:n.2139+412_2139+417delinsCTTTTG
NM_001136129.2:c.1818+412_1818+417delinsCTTTTG	NP_001129601.1:n.1818+412_1818+417delinsCTTTTG
NM_001136130.2:c.2043+412_2043+417delinsCTTTTG	NP_001129602.1:n.2043+412_2043+417delinsCTTTTG
NM_001136131.2:c.1881+412_1881+417delinsCTTTTG	NP_001129603.1:n.1881+412_1881+417delinsCTTTTG
NM_001204301.1:c.2157+412_2157+417delinsCTTTTG	NP_001191230.1:n.2157+412_2157+417delinsCTTTTG
NM_001204302.1:c.2100+412_2100+417delinsCTTTTG	NP_001191231.1:n.2100+412_2100+417delinsCTTTTG
NM_001204303.1:c.1932+412_1932+417delinsCTTTTG	NP_001191232.1:n.1932+412_1932+417delinsCTTTTG
NM_201413.2:c.2154+412_2154+417delinsCTTTTG	NP_958816.1:n.2154+412_2154+417delinsCTTTTG
NM_201414.2:c.1986+412_1986+417delinsCTTTTG	NP_958817.1:n.1986+412_1986+417delinsCTTTTG
NM_000484.4:c.2211+412_2211+417delinsCTTTTG MANE Select	NP_000475.1:n.2211+412_2211+417delinsCTTTTG
NM_001136129.3:c.1818+412_1818+417delinsCTTTTG	NP_001129601.1:n.1818+412_1818+417delinsCTTTTG
NM_001136130.3:c.2043+412_2043+417delinsCTTTTG	NP_001129602.1:n.2043+412_2043+417delinsCTTTTG
NM_001204301.2:c.2157+412_2157+417delinsCTTTTG	NP_001191230.1:n.2157+412_2157+417delinsCTTTTG
NM_001204302.2:c.2100+412_2100+417delinsCTTTTG	NP_001191231.1:n.2100+412_2100+417delinsCTTTTG
NM_001204303.2:c.1932+412_1932+417delinsCTTTTG	NP_001191232.1:n.1932+412_1932+417delinsCTTTTG
NM_201413.3:c.2154+412_2154+417delinsCTTTTG	NP_958816.1:n.2154+412_2154+417delinsCTTTTG
NM_201414.3:c.1986+412_1986+417delinsCTTTTG	NP_958817.1:n.1986+412_1986+417delinsCTTTTG
NM_001136131.3:c.1881+412_1881+417delinsCTTTTG	NP_001129603.1:n.1881+412_1881+417delinsCTTTTG
NM_001385253.1:c.2043+412_2043+417delinsCTTTTG	NP_001372182.1:n.2043+412_2043+417delinsCTTTTG