Canonical Allele Identifier: CA2654123599

Gene: APP

Linked Data

• gnomAD v4: 21-25897774-C-CTTCAAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897775_25897776insTCAAGGT , CM000683.2:g.25897775_25897776insTCAAGGT	GRCh38
NC_000021.8:g.27270087_27270088insTCAAGGT , CM000683.1:g.27270087_27270088insTCAAGGT	GRCh37
NC_000021.7:g.26191958_26191959insTCAAGGT	NCBI36
NG_007376.1:g.278046_278047insCCTTGAA
NG_007376.2:g.278354_278355insCCTTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1931-102_1931-101insCCTTGAA
ENST00000707133.1:n.361-102_361-101insCCTTGAA
ENST00000707134.1:n.630-102_630-101insCCTTGAA
ENST00000346798.8:c.1964-102_1964-101insCCTTGAA MANE Select	ENSP00000284981.4:n.1964-102_1964-101insCCTTGAA
ENST00000346798.7:c.1964-102_1964-101insCCTTGAA	ENSP00000284981.4:n.1964-102_1964-101insCCTTGAA
ENST00000348990.9:c.1739-102_1739-101insCCTTGAA	ENSP00000345463.5:n.1739-102_1739-101insCCTTGAA
ENST00000354192.7:c.1571-102_1571-101insCCTTGAA	ENSP00000346129.3:n.1571-102_1571-101insCCTTGAA
ENST00000357903.7:c.1907-102_1907-101insCCTTGAA	ENSP00000350578.3:n.1907-102_1907-101insCCTTGAA
ENST00000358918.7:c.1910-102_1910-101insCCTTGAA	ENSP00000351796.3:n.1910-102_1910-101insCCTTGAA
ENST00000359726.7:c.1634-102_1634-101insCCTTGAA	ENSP00000352760.4:n.1634-102_1634-101insCCTTGAA
ENST00000439274.6:c.1796-102_1796-101insCCTTGAA	ENSP00000398879.2:n.1796-102_1796-101insCCTTGAA
ENST00000440126.7:c.1892-102_1892-101insCCTTGAA	ENSP00000387483.2:n.1892-102_1892-101insCCTTGAA
ENST00000464867.1:n.209_210insCCTTGAA
NM_000484.3:c.1964-102_1964-101insCCTTGAA	NP_000475.1:n.1964-102_1964-101insCCTTGAA
NM_001136016.3:c.1892-102_1892-101insCCTTGAA	NP_001129488.1:n.1892-102_1892-101insCCTTGAA
NM_001136129.2:c.1571-102_1571-101insCCTTGAA	NP_001129601.1:n.1571-102_1571-101insCCTTGAA
NM_001136130.2:c.1796-102_1796-101insCCTTGAA	NP_001129602.1:n.1796-102_1796-101insCCTTGAA
NM_001136131.2:c.1634-102_1634-101insCCTTGAA	NP_001129603.1:n.1634-102_1634-101insCCTTGAA
NM_001204301.1:c.1910-102_1910-101insCCTTGAA	NP_001191230.1:n.1910-102_1910-101insCCTTGAA
NM_001204302.1:c.1853-102_1853-101insCCTTGAA	NP_001191231.1:n.1853-102_1853-101insCCTTGAA
NM_001204303.1:c.1685-102_1685-101insCCTTGAA	NP_001191232.1:n.1685-102_1685-101insCCTTGAA
NM_201413.2:c.1907-102_1907-101insCCTTGAA	NP_958816.1:n.1907-102_1907-101insCCTTGAA
NM_201414.2:c.1739-102_1739-101insCCTTGAA	NP_958817.1:n.1739-102_1739-101insCCTTGAA
NM_000484.4:c.1964-102_1964-101insCCTTGAA MANE Select	NP_000475.1:n.1964-102_1964-101insCCTTGAA
NM_001136129.3:c.1571-102_1571-101insCCTTGAA	NP_001129601.1:n.1571-102_1571-101insCCTTGAA
NM_001136130.3:c.1796-102_1796-101insCCTTGAA	NP_001129602.1:n.1796-102_1796-101insCCTTGAA
NM_001204301.2:c.1910-102_1910-101insCCTTGAA	NP_001191230.1:n.1910-102_1910-101insCCTTGAA
NM_001204302.2:c.1853-102_1853-101insCCTTGAA	NP_001191231.1:n.1853-102_1853-101insCCTTGAA
NM_001204303.2:c.1685-102_1685-101insCCTTGAA	NP_001191232.1:n.1685-102_1685-101insCCTTGAA
NM_201413.3:c.1907-102_1907-101insCCTTGAA	NP_958816.1:n.1907-102_1907-101insCCTTGAA
NM_201414.3:c.1739-102_1739-101insCCTTGAA	NP_958817.1:n.1739-102_1739-101insCCTTGAA
NM_001136131.3:c.1634-102_1634-101insCCTTGAA	NP_001129603.1:n.1634-102_1634-101insCCTTGAA
NM_001385253.1:c.1796-102_1796-101insCCTTGAA	NP_001372182.1:n.1796-102_1796-101insCCTTGAA