Canonical Allele Identifier: CA2817566482

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891406_25891410del , CM000683.2:g.25891406_25891410del	GRCh38
NC_000021.8:g.27263718_27263722del , CM000683.1:g.27263718_27263722del	GRCh37
NC_000021.7:g.26185589_26185593del	NCBI36
NG_007376.1:g.284411_284415del
NG_007376.2:g.284719_284723del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2178+312_2178+316del
ENST00000707133.1:n.608+312_608+316del
ENST00000707134.1:n.877+312_877+316del
ENST00000346798.8:c.2211+312_2211+316del MANE Select	ENSP00000284981.4:n.2211+312_2211+316del
ENST00000346798.7:c.2211+312_2211+316del	ENSP00000284981.4:n.2211+312_2211+316del
ENST00000348990.9:c.1986+312_1986+316del	ENSP00000345463.5:n.1986+312_1986+316del
ENST00000354192.7:c.1818+312_1818+316del	ENSP00000346129.3:n.1818+312_1818+316del
ENST00000357903.7:c.2154+312_2154+316del	ENSP00000350578.3:n.2154+312_2154+316del
ENST00000358918.7:c.2157+312_2157+316del	ENSP00000351796.3:n.2157+312_2157+316del
ENST00000359726.7:c.1881+312_1881+316del	ENSP00000352760.4:n.1881+312_1881+316del
ENST00000439274.6:c.2043+312_2043+316del	ENSP00000398879.2:n.2043+312_2043+316del
ENST00000440126.7:c.2139+312_2139+316del	ENSP00000387483.2:n.2139+312_2139+316del
ENST00000464867.1:n.558+312_558+316del
NM_000484.3:c.2211+312_2211+316del	NP_000475.1:n.2211+312_2211+316del
NM_001136016.3:c.2139+312_2139+316del	NP_001129488.1:n.2139+312_2139+316del
NM_001136129.2:c.1818+312_1818+316del	NP_001129601.1:n.1818+312_1818+316del
NM_001136130.2:c.2043+312_2043+316del	NP_001129602.1:n.2043+312_2043+316del
NM_001136131.2:c.1881+312_1881+316del	NP_001129603.1:n.1881+312_1881+316del
NM_001204301.1:c.2157+312_2157+316del	NP_001191230.1:n.2157+312_2157+316del
NM_001204302.1:c.2100+312_2100+316del	NP_001191231.1:n.2100+312_2100+316del
NM_001204303.1:c.1932+312_1932+316del	NP_001191232.1:n.1932+312_1932+316del
NM_201413.2:c.2154+312_2154+316del	NP_958816.1:n.2154+312_2154+316del
NM_201414.2:c.1986+312_1986+316del	NP_958817.1:n.1986+312_1986+316del
NM_000484.4:c.2211+312_2211+316del MANE Select	NP_000475.1:n.2211+312_2211+316del
NM_001136129.3:c.1818+312_1818+316del	NP_001129601.1:n.1818+312_1818+316del
NM_001136130.3:c.2043+312_2043+316del	NP_001129602.1:n.2043+312_2043+316del
NM_001204301.2:c.2157+312_2157+316del	NP_001191230.1:n.2157+312_2157+316del
NM_001204302.2:c.2100+312_2100+316del	NP_001191231.1:n.2100+312_2100+316del
NM_001204303.2:c.1932+312_1932+316del	NP_001191232.1:n.1932+312_1932+316del
NM_201413.3:c.2154+312_2154+316del	NP_958816.1:n.2154+312_2154+316del
NM_201414.3:c.1986+312_1986+316del	NP_958817.1:n.1986+312_1986+316del
NM_001136131.3:c.1881+312_1881+316del	NP_001129603.1:n.1881+312_1881+316del
NM_001385253.1:c.2043+312_2043+316del	NP_001372182.1:n.2043+312_2043+316del