Canonical Allele Identifier: CA2383555000

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897728_25897732delinsATAAT , CM000683.2:g.25897728_25897732delinsATAAT	GRCh38
NC_000021.8:g.27270040_27270044delinsATAAT , CM000683.1:g.27270040_27270044delinsATAAT	GRCh37
NC_000021.7:g.26191911_26191915delinsATAAT	NCBI36
NG_007376.1:g.278089_278093delinsATTAT
NG_007376.2:g.278397_278401delinsATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1931-59_1931-55delinsATTAT
ENST00000707133.1:n.361-59_361-55delinsATTAT
ENST00000707134.1:n.630-59_630-55delinsATTAT
ENST00000346798.8:c.1964-59_1964-55delinsATTAT MANE Select	ENSP00000284981.4:n.1964-59_1964-55delinsATTAT
ENST00000346798.7:c.1964-59_1964-55delinsATTAT	ENSP00000284981.4:n.1964-59_1964-55delinsATTAT
ENST00000348990.9:c.1739-59_1739-55delinsATTAT	ENSP00000345463.5:n.1739-59_1739-55delinsATTAT
ENST00000354192.7:c.1571-59_1571-55delinsATTAT	ENSP00000346129.3:n.1571-59_1571-55delinsATTAT
ENST00000357903.7:c.1907-59_1907-55delinsATTAT	ENSP00000350578.3:n.1907-59_1907-55delinsATTAT
ENST00000358918.7:c.1910-59_1910-55delinsATTAT	ENSP00000351796.3:n.1910-59_1910-55delinsATTAT
ENST00000359726.7:c.1634-59_1634-55delinsATTAT	ENSP00000352760.4:n.1634-59_1634-55delinsATTAT
ENST00000439274.6:c.1796-59_1796-55delinsATTAT	ENSP00000398879.2:n.1796-59_1796-55delinsATTAT
ENST00000440126.7:c.1892-59_1892-55delinsATTAT	ENSP00000387483.2:n.1892-59_1892-55delinsATTAT
ENST00000464867.1:n.252_256delinsATTAT
NM_000484.3:c.1964-59_1964-55delinsATTAT	NP_000475.1:n.1964-59_1964-55delinsATTAT
NM_001136016.3:c.1892-59_1892-55delinsATTAT	NP_001129488.1:n.1892-59_1892-55delinsATTAT
NM_001136129.2:c.1571-59_1571-55delinsATTAT	NP_001129601.1:n.1571-59_1571-55delinsATTAT
NM_001136130.2:c.1796-59_1796-55delinsATTAT	NP_001129602.1:n.1796-59_1796-55delinsATTAT
NM_001136131.2:c.1634-59_1634-55delinsATTAT	NP_001129603.1:n.1634-59_1634-55delinsATTAT
NM_001204301.1:c.1910-59_1910-55delinsATTAT	NP_001191230.1:n.1910-59_1910-55delinsATTAT
NM_001204302.1:c.1853-59_1853-55delinsATTAT	NP_001191231.1:n.1853-59_1853-55delinsATTAT
NM_001204303.1:c.1685-59_1685-55delinsATTAT	NP_001191232.1:n.1685-59_1685-55delinsATTAT
NM_201413.2:c.1907-59_1907-55delinsATTAT	NP_958816.1:n.1907-59_1907-55delinsATTAT
NM_201414.2:c.1739-59_1739-55delinsATTAT	NP_958817.1:n.1739-59_1739-55delinsATTAT
NM_000484.4:c.1964-59_1964-55delinsATTAT MANE Select	NP_000475.1:n.1964-59_1964-55delinsATTAT
NM_001136129.3:c.1571-59_1571-55delinsATTAT	NP_001129601.1:n.1571-59_1571-55delinsATTAT
NM_001136130.3:c.1796-59_1796-55delinsATTAT	NP_001129602.1:n.1796-59_1796-55delinsATTAT
NM_001204301.2:c.1910-59_1910-55delinsATTAT	NP_001191230.1:n.1910-59_1910-55delinsATTAT
NM_001204302.2:c.1853-59_1853-55delinsATTAT	NP_001191231.1:n.1853-59_1853-55delinsATTAT
NM_001204303.2:c.1685-59_1685-55delinsATTAT	NP_001191232.1:n.1685-59_1685-55delinsATTAT
NM_201413.3:c.1907-59_1907-55delinsATTAT	NP_958816.1:n.1907-59_1907-55delinsATTAT
NM_201414.3:c.1739-59_1739-55delinsATTAT	NP_958817.1:n.1739-59_1739-55delinsATTAT
NM_001136131.3:c.1634-59_1634-55delinsATTAT	NP_001129603.1:n.1634-59_1634-55delinsATTAT
NM_001385253.1:c.1796-59_1796-55delinsATTAT	NP_001372182.1:n.1796-59_1796-55delinsATTAT