Canonical Allele Identifier: CA2383555072

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897863_25897868delinsAGAAAT , CM000683.2:g.25897863_25897868delinsAGAAAT	GRCh38
NC_000021.8:g.27270175_27270180delinsAGAAAT , CM000683.1:g.27270175_27270180delinsAGAAAT	GRCh37
NC_000021.7:g.26192046_26192051delinsAGAAAT	NCBI36
NG_007376.1:g.277953_277958delinsATTTCT
NG_007376.2:g.278261_278266delinsATTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1931-195_1931-190delinsATTTCT
ENST00000707133.1:n.361-195_361-190delinsATTTCT
ENST00000707134.1:n.630-195_630-190delinsATTTCT
ENST00000346798.8:c.1964-195_1964-190delinsATTTCT MANE Select	ENSP00000284981.4:n.1964-195_1964-190delinsATTTCT
ENST00000346798.7:c.1964-195_1964-190delinsATTTCT	ENSP00000284981.4:n.1964-195_1964-190delinsATTTCT
ENST00000348990.9:c.1739-195_1739-190delinsATTTCT	ENSP00000345463.5:n.1739-195_1739-190delinsATTTCT
ENST00000354192.7:c.1571-195_1571-190delinsATTTCT	ENSP00000346129.3:n.1571-195_1571-190delinsATTTCT
ENST00000357903.7:c.1907-195_1907-190delinsATTTCT	ENSP00000350578.3:n.1907-195_1907-190delinsATTTCT
ENST00000358918.7:c.1910-195_1910-190delinsATTTCT	ENSP00000351796.3:n.1910-195_1910-190delinsATTTCT
ENST00000359726.7:c.1634-195_1634-190delinsATTTCT	ENSP00000352760.4:n.1634-195_1634-190delinsATTTCT
ENST00000439274.6:c.1796-195_1796-190delinsATTTCT	ENSP00000398879.2:n.1796-195_1796-190delinsATTTCT
ENST00000440126.7:c.1892-195_1892-190delinsATTTCT	ENSP00000387483.2:n.1892-195_1892-190delinsATTTCT
ENST00000464867.1:n.116_121delinsATTTCT
NM_000484.3:c.1964-195_1964-190delinsATTTCT	NP_000475.1:n.1964-195_1964-190delinsATTTCT
NM_001136016.3:c.1892-195_1892-190delinsATTTCT	NP_001129488.1:n.1892-195_1892-190delinsATTTCT
NM_001136129.2:c.1571-195_1571-190delinsATTTCT	NP_001129601.1:n.1571-195_1571-190delinsATTTCT
NM_001136130.2:c.1796-195_1796-190delinsATTTCT	NP_001129602.1:n.1796-195_1796-190delinsATTTCT
NM_001136131.2:c.1634-195_1634-190delinsATTTCT	NP_001129603.1:n.1634-195_1634-190delinsATTTCT
NM_001204301.1:c.1910-195_1910-190delinsATTTCT	NP_001191230.1:n.1910-195_1910-190delinsATTTCT
NM_001204302.1:c.1853-195_1853-190delinsATTTCT	NP_001191231.1:n.1853-195_1853-190delinsATTTCT
NM_001204303.1:c.1685-195_1685-190delinsATTTCT	NP_001191232.1:n.1685-195_1685-190delinsATTTCT
NM_201413.2:c.1907-195_1907-190delinsATTTCT	NP_958816.1:n.1907-195_1907-190delinsATTTCT
NM_201414.2:c.1739-195_1739-190delinsATTTCT	NP_958817.1:n.1739-195_1739-190delinsATTTCT
NM_000484.4:c.1964-195_1964-190delinsATTTCT MANE Select	NP_000475.1:n.1964-195_1964-190delinsATTTCT
NM_001136129.3:c.1571-195_1571-190delinsATTTCT	NP_001129601.1:n.1571-195_1571-190delinsATTTCT
NM_001136130.3:c.1796-195_1796-190delinsATTTCT	NP_001129602.1:n.1796-195_1796-190delinsATTTCT
NM_001204301.2:c.1910-195_1910-190delinsATTTCT	NP_001191230.1:n.1910-195_1910-190delinsATTTCT
NM_001204302.2:c.1853-195_1853-190delinsATTTCT	NP_001191231.1:n.1853-195_1853-190delinsATTTCT
NM_001204303.2:c.1685-195_1685-190delinsATTTCT	NP_001191232.1:n.1685-195_1685-190delinsATTTCT
NM_201413.3:c.1907-195_1907-190delinsATTTCT	NP_958816.1:n.1907-195_1907-190delinsATTTCT
NM_201414.3:c.1739-195_1739-190delinsATTTCT	NP_958817.1:n.1739-195_1739-190delinsATTTCT
NM_001136131.3:c.1634-195_1634-190delinsATTTCT	NP_001129603.1:n.1634-195_1634-190delinsATTTCT
NM_001385253.1:c.1796-195_1796-190delinsATTTCT	NP_001372182.1:n.1796-195_1796-190delinsATTTCT