Canonical Allele Identifier: CA2383551654
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891877_25891882delinsCAAATT , CM000683.2:g.25891877_25891882delinsCAAATT GRCh38
NC_000021.8:g.27264189_27264194delinsCAAATT , CM000683.1:g.27264189_27264194delinsCAAATT GRCh37
NC_000021.7:g.26186060_26186065delinsCAAATT NCBI36
NG_007376.1:g.283939_283944delinsAATTTG
NG_007376.2:g.284247_284252delinsAATTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2032-14_2032-9delinsAATTTG
ENST00000707133.1:n.462-14_462-9delinsAATTTG
ENST00000707134.1:n.731-14_731-9delinsAATTTG
ENST00000346798.8:c.2065-14_2065-9delinsAATTTG MANE Select ENSP00000284981.4:n.2065-14_2065-9delinsA...
ENST00000346798.7:c.2065-14_2065-9delinsAATTTG ENSP00000284981.4:n.2065-14_2065-9delinsA...
ENST00000348990.9:c.1840-14_1840-9delinsAATTTG ENSP00000345463.5:n.1840-14_1840-9delinsA...
ENST00000354192.7:c.1672-14_1672-9delinsAATTTG ENSP00000346129.3:n.1672-14_1672-9delinsA...
ENST00000357903.7:c.2008-14_2008-9delinsAATTTG ENSP00000350578.3:n.2008-14_2008-9delinsA...
ENST00000358918.7:c.2011-14_2011-9delinsAATTTG ENSP00000351796.3:n.2011-14_2011-9delinsA...
ENST00000359726.7:c.1735-14_1735-9delinsAATTTG ENSP00000352760.4:n.1735-14_1735-9delinsA...
ENST00000439274.6:c.1897-14_1897-9delinsAATTTG ENSP00000398879.2:n.1897-14_1897-9delinsA...
ENST00000440126.7:c.1993-14_1993-9delinsAATTTG ENSP00000387483.2:n.1993-14_1993-9delinsA...
ENST00000464867.1:n.412-14_412-9delinsAATTTG
NM_000484.3:c.2065-14_2065-9delinsAATTTG NP_000475.1:n.2065-14_2065-9delinsAATTTG
NM_001136016.3:c.1993-14_1993-9delinsAATTTG NP_001129488.1:n.1993-14_1993-9delinsAATT...
NM_001136129.2:c.1672-14_1672-9delinsAATTTG NP_001129601.1:n.1672-14_1672-9delinsAATT...
NM_001136130.2:c.1897-14_1897-9delinsAATTTG NP_001129602.1:n.1897-14_1897-9delinsAATT...
NM_001136131.2:c.1735-14_1735-9delinsAATTTG NP_001129603.1:n.1735-14_1735-9delinsAATT...
NM_001204301.1:c.2011-14_2011-9delinsAATTTG NP_001191230.1:n.2011-14_2011-9delinsAATT...
NM_001204302.1:c.1954-14_1954-9delinsAATTTG NP_001191231.1:n.1954-14_1954-9delinsAATT...
NM_001204303.1:c.1786-14_1786-9delinsAATTTG NP_001191232.1:n.1786-14_1786-9delinsAATT...
NM_201413.2:c.2008-14_2008-9delinsAATTTG NP_958816.1:n.2008-14_2008-9delinsAATTTG
NM_201414.2:c.1840-14_1840-9delinsAATTTG NP_958817.1:n.1840-14_1840-9delinsAATTTG
NM_000484.4:c.2065-14_2065-9delinsAATTTG MANE Select NP_000475.1:n.2065-14_2065-9delinsAATTTG
NM_001136129.3:c.1672-14_1672-9delinsAATTTG NP_001129601.1:n.1672-14_1672-9delinsAATT...
NM_001136130.3:c.1897-14_1897-9delinsAATTTG NP_001129602.1:n.1897-14_1897-9delinsAATT...
NM_001204301.2:c.2011-14_2011-9delinsAATTTG NP_001191230.1:n.2011-14_2011-9delinsAATT...
NM_001204302.2:c.1954-14_1954-9delinsAATTTG NP_001191231.1:n.1954-14_1954-9delinsAATT...
NM_001204303.2:c.1786-14_1786-9delinsAATTTG NP_001191232.1:n.1786-14_1786-9delinsAATT...
NM_201413.3:c.2008-14_2008-9delinsAATTTG NP_958816.1:n.2008-14_2008-9delinsAATTTG
NM_201414.3:c.1840-14_1840-9delinsAATTTG NP_958817.1:n.1840-14_1840-9delinsAATTTG
NM_001136131.3:c.1735-14_1735-9delinsAATTTG NP_001129603.1:n.1735-14_1735-9delinsAATT...
NM_001385253.1:c.1897-14_1897-9delinsAATTTG NP_001372182.1:n.1897-14_1897-9delinsAATT...