Canonical Allele Identifier: CA2533073910

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897955_25897956insTTAAATATAGGGTATC , CM000683.2:g.25897955_25897956insTTAAATATAGGGTATC	GRCh38
NC_000021.8:g.27270267_27270268insTTAAATATAGGGTATC , CM000683.1:g.27270267_27270268insTTAAATATAGGGTATC	GRCh37
NC_000021.7:g.26192138_26192139insTTAAATATAGGGTATC	NCBI36
NG_007376.1:g.277865_277866insGATACCCTATATTTAA
NG_007376.2:g.278173_278174insGATACCCTATATTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1931-283_1931-282insGATACCCTATATTTAA
ENST00000707133.1:n.361-283_361-282insGATACCCTATATTTAA
ENST00000707134.1:n.630-283_630-282insGATACCCTATATTTAA
ENST00000346798.8:c.1964-283_1964-282insGATACCCTATATTTAA MANE Select	ENSP00000284981.4:n.1964-283_1964-282insGATACCCTATATTTAA
ENST00000346798.7:c.1964-283_1964-282insGATACCCTATATTTAA	ENSP00000284981.4:n.1964-283_1964-282insGATACCCTATATTTAA
ENST00000348990.9:c.1739-283_1739-282insGATACCCTATATTTAA	ENSP00000345463.5:n.1739-283_1739-282insGATACCCTATATTTAA
ENST00000354192.7:c.1571-283_1571-282insGATACCCTATATTTAA	ENSP00000346129.3:n.1571-283_1571-282insGATACCCTATATTTAA
ENST00000357903.7:c.1907-283_1907-282insGATACCCTATATTTAA	ENSP00000350578.3:n.1907-283_1907-282insGATACCCTATATTTAA
ENST00000358918.7:c.1910-283_1910-282insGATACCCTATATTTAA	ENSP00000351796.3:n.1910-283_1910-282insGATACCCTATATTTAA
ENST00000359726.7:c.1634-283_1634-282insGATACCCTATATTTAA	ENSP00000352760.4:n.1634-283_1634-282insGATACCCTATATTTAA
ENST00000439274.6:c.1796-283_1796-282insGATACCCTATATTTAA	ENSP00000398879.2:n.1796-283_1796-282insGATACCCTATATTTAA
ENST00000440126.7:c.1892-283_1892-282insGATACCCTATATTTAA	ENSP00000387483.2:n.1892-283_1892-282insGATACCCTATATTTAA
ENST00000464867.1:n.28_29insGATACCCTATATTTAA
NM_000484.3:c.1964-283_1964-282insGATACCCTATATTTAA	NP_000475.1:n.1964-283_1964-282insGATACCCTATATTTAA
NM_001136016.3:c.1892-283_1892-282insGATACCCTATATTTAA	NP_001129488.1:n.1892-283_1892-282insGATACCCTATATTTAA
NM_001136129.2:c.1571-283_1571-282insGATACCCTATATTTAA	NP_001129601.1:n.1571-283_1571-282insGATACCCTATATTTAA
NM_001136130.2:c.1796-283_1796-282insGATACCCTATATTTAA	NP_001129602.1:n.1796-283_1796-282insGATACCCTATATTTAA
NM_001136131.2:c.1634-283_1634-282insGATACCCTATATTTAA	NP_001129603.1:n.1634-283_1634-282insGATACCCTATATTTAA
NM_001204301.1:c.1910-283_1910-282insGATACCCTATATTTAA	NP_001191230.1:n.1910-283_1910-282insGATACCCTATATTTAA
NM_001204302.1:c.1853-283_1853-282insGATACCCTATATTTAA	NP_001191231.1:n.1853-283_1853-282insGATACCCTATATTTAA
NM_001204303.1:c.1685-283_1685-282insGATACCCTATATTTAA	NP_001191232.1:n.1685-283_1685-282insGATACCCTATATTTAA
NM_201413.2:c.1907-283_1907-282insGATACCCTATATTTAA	NP_958816.1:n.1907-283_1907-282insGATACCCTATATTTAA
NM_201414.2:c.1739-283_1739-282insGATACCCTATATTTAA	NP_958817.1:n.1739-283_1739-282insGATACCCTATATTTAA
NM_000484.4:c.1964-283_1964-282insGATACCCTATATTTAA MANE Select	NP_000475.1:n.1964-283_1964-282insGATACCCTATATTTAA
NM_001136129.3:c.1571-283_1571-282insGATACCCTATATTTAA	NP_001129601.1:n.1571-283_1571-282insGATACCCTATATTTAA
NM_001136130.3:c.1796-283_1796-282insGATACCCTATATTTAA	NP_001129602.1:n.1796-283_1796-282insGATACCCTATATTTAA
NM_001204301.2:c.1910-283_1910-282insGATACCCTATATTTAA	NP_001191230.1:n.1910-283_1910-282insGATACCCTATATTTAA
NM_001204302.2:c.1853-283_1853-282insGATACCCTATATTTAA	NP_001191231.1:n.1853-283_1853-282insGATACCCTATATTTAA
NM_001204303.2:c.1685-283_1685-282insGATACCCTATATTTAA	NP_001191232.1:n.1685-283_1685-282insGATACCCTATATTTAA
NM_201413.3:c.1907-283_1907-282insGATACCCTATATTTAA	NP_958816.1:n.1907-283_1907-282insGATACCCTATATTTAA
NM_201414.3:c.1739-283_1739-282insGATACCCTATATTTAA	NP_958817.1:n.1739-283_1739-282insGATACCCTATATTTAA
NM_001136131.3:c.1634-283_1634-282insGATACCCTATATTTAA	NP_001129603.1:n.1634-283_1634-282insGATACCCTATATTTAA
NM_001385253.1:c.1796-283_1796-282insGATACCCTATATTTAA	NP_001372182.1:n.1796-283_1796-282insGATACCCTATATTTAA