Canonical Allele Identifier: CA319097409

Gene: APP

Linked Data

• dbSNP Id: rs367709245
• gnomAD v2: 21-27263945-GATACTT-G
• gnomAD v3: 21-25891633-GATACTT-G
• gnomAD v4: 21-25891633-GATACTT-G
• MyVariant Identifiers: chr21:g.27263946_27263951del (hg19) ; chr21:g.25891634_25891639del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891635_25891640del , CM000683.2:g.25891635_25891640del	GRCh38
NC_000021.8:g.27263947_27263952del , CM000683.1:g.27263947_27263952del	GRCh37
NC_000021.7:g.26185818_26185823del	NCBI36
NG_007376.1:g.284182_284187del
NG_007376.2:g.284490_284495del

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2178+83_2178+88del
ENST00000707133.1:n.608+83_608+88del
ENST00000707134.1:n.877+83_877+88del
ENST00000346798.8:c.2211+83_2211+88del MANE Select	ENSP00000284981.4:n.2211+83_2211+88del
ENST00000346798.7:c.2211+83_2211+88del	ENSP00000284981.4:n.2211+83_2211+88del
ENST00000348990.9:c.1986+83_1986+88del	ENSP00000345463.5:n.1986+83_1986+88del
ENST00000354192.7:c.1818+83_1818+88del	ENSP00000346129.3:n.1818+83_1818+88del
ENST00000357903.7:c.2154+83_2154+88del	ENSP00000350578.3:n.2154+83_2154+88del
ENST00000358918.7:c.2157+83_2157+88del	ENSP00000351796.3:n.2157+83_2157+88del
ENST00000359726.7:c.1881+83_1881+88del	ENSP00000352760.4:n.1881+83_1881+88del
ENST00000439274.6:c.2043+83_2043+88del	ENSP00000398879.2:n.2043+83_2043+88del
ENST00000440126.7:c.2139+83_2139+88del	ENSP00000387483.2:n.2139+83_2139+88del
ENST00000464867.1:n.558+83_558+88del
NM_000484.3:c.2211+83_2211+88del	NP_000475.1:n.2211+83_2211+88del
NM_001136016.3:c.2139+83_2139+88del	NP_001129488.1:n.2139+83_2139+88del
NM_001136129.2:c.1818+83_1818+88del	NP_001129601.1:n.1818+83_1818+88del
NM_001136130.2:c.2043+83_2043+88del	NP_001129602.1:n.2043+83_2043+88del
NM_001136131.2:c.1881+83_1881+88del	NP_001129603.1:n.1881+83_1881+88del
NM_001204301.1:c.2157+83_2157+88del	NP_001191230.1:n.2157+83_2157+88del
NM_001204302.1:c.2100+83_2100+88del	NP_001191231.1:n.2100+83_2100+88del
NM_001204303.1:c.1932+83_1932+88del	NP_001191232.1:n.1932+83_1932+88del
NM_201413.2:c.2154+83_2154+88del	NP_958816.1:n.2154+83_2154+88del
NM_201414.2:c.1986+83_1986+88del	NP_958817.1:n.1986+83_1986+88del
NM_000484.4:c.2211+83_2211+88del MANE Select	NP_000475.1:n.2211+83_2211+88del
NM_001136129.3:c.1818+83_1818+88del	NP_001129601.1:n.1818+83_1818+88del
NM_001136130.3:c.2043+83_2043+88del	NP_001129602.1:n.2043+83_2043+88del
NM_001204301.2:c.2157+83_2157+88del	NP_001191230.1:n.2157+83_2157+88del
NM_001204302.2:c.2100+83_2100+88del	NP_001191231.1:n.2100+83_2100+88del
NM_001204303.2:c.1932+83_1932+88del	NP_001191232.1:n.1932+83_1932+88del
NM_201413.3:c.2154+83_2154+88del	NP_958816.1:n.2154+83_2154+88del
NM_201414.3:c.1986+83_1986+88del	NP_958817.1:n.1986+83_1986+88del
NM_001136131.3:c.1881+83_1881+88del	NP_001129603.1:n.1881+83_1881+88del
NM_001385253.1:c.2043+83_2043+88del	NP_001372182.1:n.2043+83_2043+88del