Canonical Allele Identifier: CA637162686

Gene: APP

Linked Data

• dbSNP Id: rs1256953047
• gnomAD v2: 21-27263982-TTC-T
• gnomAD v4: 21-25891670-TTC-T
• MyVariant Identifiers: chr21:g.27263983_27263984del (hg19) ; chr21:g.25891671_25891672del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891675_25891676del , CM000683.2:g.25891675_25891676del	GRCh38
NC_000021.8:g.27263987_27263988del , CM000683.1:g.27263987_27263988del	GRCh37
NC_000021.7:g.26185858_26185859del	NCBI36
NG_007376.1:g.284149_284150del
NG_007376.2:g.284457_284458del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2178+50_2178+51del
ENST00000707133.1:n.608+50_608+51del
ENST00000707134.1:n.877+50_877+51del
ENST00000346798.8:c.2211+50_2211+51del MANE Select	ENSP00000284981.4:n.2211+50_2211+51del
ENST00000346798.7:c.2211+50_2211+51del	ENSP00000284981.4:n.2211+50_2211+51del
ENST00000348990.9:c.1986+50_1986+51del	ENSP00000345463.5:n.1986+50_1986+51del
ENST00000354192.7:c.1818+50_1818+51del	ENSP00000346129.3:n.1818+50_1818+51del
ENST00000357903.7:c.2154+50_2154+51del	ENSP00000350578.3:n.2154+50_2154+51del
ENST00000358918.7:c.2157+50_2157+51del	ENSP00000351796.3:n.2157+50_2157+51del
ENST00000359726.7:c.1881+50_1881+51del	ENSP00000352760.4:n.1881+50_1881+51del
ENST00000439274.6:c.2043+50_2043+51del	ENSP00000398879.2:n.2043+50_2043+51del
ENST00000440126.7:c.2139+50_2139+51del	ENSP00000387483.2:n.2139+50_2139+51del
ENST00000464867.1:n.558+50_558+51del
NM_000484.3:c.2211+50_2211+51del	NP_000475.1:n.2211+50_2211+51del
NM_001136016.3:c.2139+50_2139+51del	NP_001129488.1:n.2139+50_2139+51del
NM_001136129.2:c.1818+50_1818+51del	NP_001129601.1:n.1818+50_1818+51del
NM_001136130.2:c.2043+50_2043+51del	NP_001129602.1:n.2043+50_2043+51del
NM_001136131.2:c.1881+50_1881+51del	NP_001129603.1:n.1881+50_1881+51del
NM_001204301.1:c.2157+50_2157+51del	NP_001191230.1:n.2157+50_2157+51del
NM_001204302.1:c.2100+50_2100+51del	NP_001191231.1:n.2100+50_2100+51del
NM_001204303.1:c.1932+50_1932+51del	NP_001191232.1:n.1932+50_1932+51del
NM_201413.2:c.2154+50_2154+51del	NP_958816.1:n.2154+50_2154+51del
NM_201414.2:c.1986+50_1986+51del	NP_958817.1:n.1986+50_1986+51del
NM_000484.4:c.2211+50_2211+51del MANE Select	NP_000475.1:n.2211+50_2211+51del
NM_001136129.3:c.1818+50_1818+51del	NP_001129601.1:n.1818+50_1818+51del
NM_001136130.3:c.2043+50_2043+51del	NP_001129602.1:n.2043+50_2043+51del
NM_001204301.2:c.2157+50_2157+51del	NP_001191230.1:n.2157+50_2157+51del
NM_001204302.2:c.2100+50_2100+51del	NP_001191231.1:n.2100+50_2100+51del
NM_001204303.2:c.1932+50_1932+51del	NP_001191232.1:n.1932+50_1932+51del
NM_201413.3:c.2154+50_2154+51del	NP_958816.1:n.2154+50_2154+51del
NM_201414.3:c.1986+50_1986+51del	NP_958817.1:n.1986+50_1986+51del
NM_001136131.3:c.1881+50_1881+51del	NP_001129603.1:n.1881+50_1881+51del
NM_001385253.1:c.2043+50_2043+51del	NP_001372182.1:n.2043+50_2043+51del