Canonical Allele Identifier: CA2654123556

Gene: APP

Linked Data

• gnomAD v4: 21-25897750-CCTACCCAAAACTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897753_25897765del , CM000683.2:g.25897753_25897765del	GRCh38
NC_000021.8:g.27270065_27270077del , CM000683.1:g.27270065_27270077del	GRCh37
NC_000021.7:g.26191936_26191948del	NCBI36
NG_007376.1:g.278058_278070del
NG_007376.2:g.278366_278378del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1931-90_1931-78del
ENST00000707133.1:n.361-90_361-78del
ENST00000707134.1:n.630-90_630-78del
ENST00000346798.8:c.1964-90_1964-78del MANE Select	ENSP00000284981.4:n.1964-90_1964-78del
ENST00000346798.7:c.1964-90_1964-78del	ENSP00000284981.4:n.1964-90_1964-78del
ENST00000348990.9:c.1739-90_1739-78del	ENSP00000345463.5:n.1739-90_1739-78del
ENST00000354192.7:c.1571-90_1571-78del	ENSP00000346129.3:n.1571-90_1571-78del
ENST00000357903.7:c.1907-90_1907-78del	ENSP00000350578.3:n.1907-90_1907-78del
ENST00000358918.7:c.1910-90_1910-78del	ENSP00000351796.3:n.1910-90_1910-78del
ENST00000359726.7:c.1634-90_1634-78del	ENSP00000352760.4:n.1634-90_1634-78del
ENST00000439274.6:c.1796-90_1796-78del	ENSP00000398879.2:n.1796-90_1796-78del
ENST00000440126.7:c.1892-90_1892-78del	ENSP00000387483.2:n.1892-90_1892-78del
ENST00000464867.1:n.221_233del
NM_000484.3:c.1964-90_1964-78del	NP_000475.1:n.1964-90_1964-78del
NM_001136016.3:c.1892-90_1892-78del	NP_001129488.1:n.1892-90_1892-78del
NM_001136129.2:c.1571-90_1571-78del	NP_001129601.1:n.1571-90_1571-78del
NM_001136130.2:c.1796-90_1796-78del	NP_001129602.1:n.1796-90_1796-78del
NM_001136131.2:c.1634-90_1634-78del	NP_001129603.1:n.1634-90_1634-78del
NM_001204301.1:c.1910-90_1910-78del	NP_001191230.1:n.1910-90_1910-78del
NM_001204302.1:c.1853-90_1853-78del	NP_001191231.1:n.1853-90_1853-78del
NM_001204303.1:c.1685-90_1685-78del	NP_001191232.1:n.1685-90_1685-78del
NM_201413.2:c.1907-90_1907-78del	NP_958816.1:n.1907-90_1907-78del
NM_201414.2:c.1739-90_1739-78del	NP_958817.1:n.1739-90_1739-78del
NM_000484.4:c.1964-90_1964-78del MANE Select	NP_000475.1:n.1964-90_1964-78del
NM_001136129.3:c.1571-90_1571-78del	NP_001129601.1:n.1571-90_1571-78del
NM_001136130.3:c.1796-90_1796-78del	NP_001129602.1:n.1796-90_1796-78del
NM_001204301.2:c.1910-90_1910-78del	NP_001191230.1:n.1910-90_1910-78del
NM_001204302.2:c.1853-90_1853-78del	NP_001191231.1:n.1853-90_1853-78del
NM_001204303.2:c.1685-90_1685-78del	NP_001191232.1:n.1685-90_1685-78del
NM_201413.3:c.1907-90_1907-78del	NP_958816.1:n.1907-90_1907-78del
NM_201414.3:c.1739-90_1739-78del	NP_958817.1:n.1739-90_1739-78del
NM_001136131.3:c.1634-90_1634-78del	NP_001129603.1:n.1634-90_1634-78del
NM_001385253.1:c.1796-90_1796-78del	NP_001372182.1:n.1796-90_1796-78del