Canonical Allele Identifier: CA2383555181

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25898078_25898079delinsTA , CM000683.2:g.25898078_25898079delinsTA	GRCh38
NC_000021.8:g.27270390_27270391delinsTA , CM000683.1:g.27270390_27270391delinsTA	GRCh37
NC_000021.7:g.26192261_26192262delinsTA	NCBI36
NG_007376.1:g.277742_277743delinsTA
NG_007376.2:g.278050_278051delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1931-406_1931-405delinsTA
ENST00000707133.1:n.361-406_361-405delinsTA
ENST00000707134.1:n.630-406_630-405delinsTA
ENST00000346798.8:c.1964-406_1964-405delinsTA MANE Select	ENSP00000284981.4:n.1964-406_1964-405delinsTA
ENST00000346798.7:c.1964-406_1964-405delinsTA	ENSP00000284981.4:n.1964-406_1964-405delinsTA
ENST00000348990.9:c.1739-406_1739-405delinsTA	ENSP00000345463.5:n.1739-406_1739-405delinsTA
ENST00000354192.7:c.1571-406_1571-405delinsTA	ENSP00000346129.3:n.1571-406_1571-405delinsTA
ENST00000357903.7:c.1907-406_1907-405delinsTA	ENSP00000350578.3:n.1907-406_1907-405delinsTA
ENST00000358918.7:c.1910-406_1910-405delinsTA	ENSP00000351796.3:n.1910-406_1910-405delinsTA
ENST00000359726.7:c.1634-406_1634-405delinsTA	ENSP00000352760.4:n.1634-406_1634-405delinsTA
ENST00000439274.6:c.1796-406_1796-405delinsTA	ENSP00000398879.2:n.1796-406_1796-405delinsTA
ENST00000440126.7:c.1892-406_1892-405delinsTA	ENSP00000387483.2:n.1892-406_1892-405delinsTA
NM_000484.3:c.1964-406_1964-405delinsTA	NP_000475.1:n.1964-406_1964-405delinsTA
NM_001136016.3:c.1892-406_1892-405delinsTA	NP_001129488.1:n.1892-406_1892-405delinsTA
NM_001136129.2:c.1571-406_1571-405delinsTA	NP_001129601.1:n.1571-406_1571-405delinsTA
NM_001136130.2:c.1796-406_1796-405delinsTA	NP_001129602.1:n.1796-406_1796-405delinsTA
NM_001136131.2:c.1634-406_1634-405delinsTA	NP_001129603.1:n.1634-406_1634-405delinsTA
NM_001204301.1:c.1910-406_1910-405delinsTA	NP_001191230.1:n.1910-406_1910-405delinsTA
NM_001204302.1:c.1853-406_1853-405delinsTA	NP_001191231.1:n.1853-406_1853-405delinsTA
NM_001204303.1:c.1685-406_1685-405delinsTA	NP_001191232.1:n.1685-406_1685-405delinsTA
NM_201413.2:c.1907-406_1907-405delinsTA	NP_958816.1:n.1907-406_1907-405delinsTA
NM_201414.2:c.1739-406_1739-405delinsTA	NP_958817.1:n.1739-406_1739-405delinsTA
NM_000484.4:c.1964-406_1964-405delinsTA MANE Select	NP_000475.1:n.1964-406_1964-405delinsTA
NM_001136129.3:c.1571-406_1571-405delinsTA	NP_001129601.1:n.1571-406_1571-405delinsTA
NM_001136130.3:c.1796-406_1796-405delinsTA	NP_001129602.1:n.1796-406_1796-405delinsTA
NM_001204301.2:c.1910-406_1910-405delinsTA	NP_001191230.1:n.1910-406_1910-405delinsTA
NM_001204302.2:c.1853-406_1853-405delinsTA	NP_001191231.1:n.1853-406_1853-405delinsTA
NM_001204303.2:c.1685-406_1685-405delinsTA	NP_001191232.1:n.1685-406_1685-405delinsTA
NM_201413.3:c.1907-406_1907-405delinsTA	NP_958816.1:n.1907-406_1907-405delinsTA
NM_201414.3:c.1739-406_1739-405delinsTA	NP_958817.1:n.1739-406_1739-405delinsTA
NM_001136131.3:c.1634-406_1634-405delinsTA	NP_001129603.1:n.1634-406_1634-405delinsTA
NM_001385253.1:c.1796-406_1796-405delinsTA	NP_001372182.1:n.1796-406_1796-405delinsTA