Canonical Allele Identifier: CA2383551438

Gene: APP

Linked Data

• dbSNP Id: rs2037687928

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891423_25891424del , CM000683.2:g.25891423_25891424del	GRCh38
NC_000021.8:g.27263735_27263736del , CM000683.1:g.27263735_27263736del	GRCh37
NC_000021.7:g.26185606_26185607del	NCBI36
NG_007376.1:g.284398_284399del
NG_007376.2:g.284706_284707del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2178+299_2178+300del
ENST00000707133.1:n.608+299_608+300del
ENST00000707134.1:n.877+299_877+300del
ENST00000346798.8:c.2211+299_2211+300del MANE Select	ENSP00000284981.4:n.2211+299_2211+300del
ENST00000346798.7:c.2211+299_2211+300del	ENSP00000284981.4:n.2211+299_2211+300del
ENST00000348990.9:c.1986+299_1986+300del	ENSP00000345463.5:n.1986+299_1986+300del
ENST00000354192.7:c.1818+299_1818+300del	ENSP00000346129.3:n.1818+299_1818+300del
ENST00000357903.7:c.2154+299_2154+300del	ENSP00000350578.3:n.2154+299_2154+300del
ENST00000358918.7:c.2157+299_2157+300del	ENSP00000351796.3:n.2157+299_2157+300del
ENST00000359726.7:c.1881+299_1881+300del	ENSP00000352760.4:n.1881+299_1881+300del
ENST00000439274.6:c.2043+299_2043+300del	ENSP00000398879.2:n.2043+299_2043+300del
ENST00000440126.7:c.2139+299_2139+300del	ENSP00000387483.2:n.2139+299_2139+300del
ENST00000464867.1:n.558+299_558+300del
NM_000484.3:c.2211+299_2211+300del	NP_000475.1:n.2211+299_2211+300del
NM_001136016.3:c.2139+299_2139+300del	NP_001129488.1:n.2139+299_2139+300del
NM_001136129.2:c.1818+299_1818+300del	NP_001129601.1:n.1818+299_1818+300del
NM_001136130.2:c.2043+299_2043+300del	NP_001129602.1:n.2043+299_2043+300del
NM_001136131.2:c.1881+299_1881+300del	NP_001129603.1:n.1881+299_1881+300del
NM_001204301.1:c.2157+299_2157+300del	NP_001191230.1:n.2157+299_2157+300del
NM_001204302.1:c.2100+299_2100+300del	NP_001191231.1:n.2100+299_2100+300del
NM_001204303.1:c.1932+299_1932+300del	NP_001191232.1:n.1932+299_1932+300del
NM_201413.2:c.2154+299_2154+300del	NP_958816.1:n.2154+299_2154+300del
NM_201414.2:c.1986+299_1986+300del	NP_958817.1:n.1986+299_1986+300del
NM_000484.4:c.2211+299_2211+300del MANE Select	NP_000475.1:n.2211+299_2211+300del
NM_001136129.3:c.1818+299_1818+300del	NP_001129601.1:n.1818+299_1818+300del
NM_001136130.3:c.2043+299_2043+300del	NP_001129602.1:n.2043+299_2043+300del
NM_001204301.2:c.2157+299_2157+300del	NP_001191230.1:n.2157+299_2157+300del
NM_001204302.2:c.2100+299_2100+300del	NP_001191231.1:n.2100+299_2100+300del
NM_001204303.2:c.1932+299_1932+300del	NP_001191232.1:n.1932+299_1932+300del
NM_201413.3:c.2154+299_2154+300del	NP_958816.1:n.2154+299_2154+300del
NM_201414.3:c.1986+299_1986+300del	NP_958817.1:n.1986+299_1986+300del
NM_001136131.3:c.1881+299_1881+300del	NP_001129603.1:n.1881+299_1881+300del
NM_001385253.1:c.2043+299_2043+300del	NP_001372182.1:n.2043+299_2043+300del