Canonical Allele Identifier: CA2383551537
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891628_25891637delinsAAAGAGATAC , CM000683.2:g.25891628_25891637delinsAAAGAGATAC GRCh38
NC_000021.8:g.27263940_27263949delinsAAAGAGATAC , CM000683.1:g.27263940_27263949delinsAAAGAGATAC GRCh37
NC_000021.7:g.26185811_26185820delinsAAAGAGATAC NCBI36
NG_007376.1:g.284184_284193delinsGTATCTCTTT
NG_007376.2:g.284492_284501delinsGTATCTCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000346798.8:c.2211+85_2211+94delinsGTATCTCTTT MANE Select ENSP00000284981.4:n.2211+85_2211+94delins...
ENST00000346798.7:c.2211+85_2211+94delinsGTATCTCTTT ENSP00000284981.4:n.2211+85_2211+94delins...
ENST00000348990.9:c.1986+85_1986+94delinsGTATCTCTTT ENSP00000345463.5:n.1986+85_1986+94delins...
ENST00000354192.7:c.1818+85_1818+94delinsGTATCTCTTT ENSP00000346129.3:n.1818+85_1818+94delins...
ENST00000357903.7:c.2154+85_2154+94delinsGTATCTCTTT ENSP00000350578.3:n.2154+85_2154+94delins...
ENST00000358918.7:c.2157+85_2157+94delinsGTATCTCTTT ENSP00000351796.3:n.2157+85_2157+94delins...
ENST00000359726.7:c.1881+85_1881+94delinsGTATCTCTTT ENSP00000352760.4:n.1881+85_1881+94delins...
ENST00000439274.6:c.2043+85_2043+94delinsGTATCTCTTT ENSP00000398879.2:n.2043+85_2043+94delins...
ENST00000440126.7:c.2139+85_2139+94delinsGTATCTCTTT ENSP00000387483.2:n.2139+85_2139+94delins...
ENST00000464867.1:n.558+85_558+94delinsGTATCTCTTT
NM_000484.3:c.2211+85_2211+94delinsGTATCTCTTT NP_000475.1:n.2211+85_2211+94delinsGTATCT...
NM_001136016.3:c.2139+85_2139+94delinsGTATCTCTTT NP_001129488.1:n.2139+85_2139+94delinsGTA...
NM_001136129.2:c.1818+85_1818+94delinsGTATCTCTTT NP_001129601.1:n.1818+85_1818+94delinsGTA...
NM_001136130.2:c.2043+85_2043+94delinsGTATCTCTTT NP_001129602.1:n.2043+85_2043+94delinsGTA...
NM_001136131.2:c.1881+85_1881+94delinsGTATCTCTTT NP_001129603.1:n.1881+85_1881+94delinsGTA...
NM_001204301.1:c.2157+85_2157+94delinsGTATCTCTTT NP_001191230.1:n.2157+85_2157+94delinsGTA...
NM_001204302.1:c.2100+85_2100+94delinsGTATCTCTTT NP_001191231.1:n.2100+85_2100+94delinsGTA...
NM_001204303.1:c.1932+85_1932+94delinsGTATCTCTTT NP_001191232.1:n.1932+85_1932+94delinsGTA...
NM_201413.2:c.2154+85_2154+94delinsGTATCTCTTT NP_958816.1:n.2154+85_2154+94delinsGTATCT...
NM_201414.2:c.1986+85_1986+94delinsGTATCTCTTT NP_958817.1:n.1986+85_1986+94delinsGTATCT...
NM_000484.4:c.2211+85_2211+94delinsGTATCTCTTT MANE Select NP_000475.1:n.2211+85_2211+94delinsGTATCT...
NM_001136129.3:c.1818+85_1818+94delinsGTATCTCTTT NP_001129601.1:n.1818+85_1818+94delinsGTA...
NM_001136130.3:c.2043+85_2043+94delinsGTATCTCTTT NP_001129602.1:n.2043+85_2043+94delinsGTA...
NM_001204301.2:c.2157+85_2157+94delinsGTATCTCTTT NP_001191230.1:n.2157+85_2157+94delinsGTA...
NM_001204302.2:c.2100+85_2100+94delinsGTATCTCTTT NP_001191231.1:n.2100+85_2100+94delinsGTA...
NM_001204303.2:c.1932+85_1932+94delinsGTATCTCTTT NP_001191232.1:n.1932+85_1932+94delinsGTA...
NM_201413.3:c.2154+85_2154+94delinsGTATCTCTTT NP_958816.1:n.2154+85_2154+94delinsGTATCT...
NM_201414.3:c.1986+85_1986+94delinsGTATCTCTTT NP_958817.1:n.1986+85_1986+94delinsGTATCT...
NM_001136131.3:c.1881+85_1881+94delinsGTATCTCTTT NP_001129603.1:n.1881+85_1881+94delinsGTA...
NM_001385253.1:c.2043+85_2043+94delinsGTATCTCTTT NP_001372182.1:n.2043+85_2043+94delinsGTA...