Canonical Allele Identifier: CA748248118

Gene: APP

Linked Data

• dbSNP Id: rs1304947284
• gnomAD v3: 21-25898098-C-CATTA
• gnomAD v4: 21-25898098-C-CATTA
• MyVariant Identifiers: chr21:g.27270410_27270411insATTA (hg19) ; chr21:g.25898098_25898099insATTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25898103_25898106dup , CM000683.2:g.25898103_25898106dup	GRCh38
NC_000021.8:g.27270415_27270418dup , CM000683.1:g.27270415_27270418dup	GRCh37
NC_000021.7:g.26192286_26192289dup	NCBI36
NG_007376.1:g.277719_277722dup
NG_007376.2:g.278027_278030dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1931-429_1931-426dup
ENST00000707133.1:n.361-429_361-426dup
ENST00000707134.1:n.630-429_630-426dup
ENST00000346798.8:c.1964-429_1964-426dup MANE Select	ENSP00000284981.4:n.1964-429_1964-426dup
ENST00000346798.7:c.1964-429_1964-426dup	ENSP00000284981.4:n.1964-429_1964-426dup
ENST00000348990.9:c.1739-429_1739-426dup	ENSP00000345463.5:n.1739-429_1739-426dup
ENST00000354192.7:c.1571-429_1571-426dup	ENSP00000346129.3:n.1571-429_1571-426dup
ENST00000357903.7:c.1907-429_1907-426dup	ENSP00000350578.3:n.1907-429_1907-426dup
ENST00000358918.7:c.1910-429_1910-426dup	ENSP00000351796.3:n.1910-429_1910-426dup
ENST00000359726.7:c.1634-429_1634-426dup	ENSP00000352760.4:n.1634-429_1634-426dup
ENST00000439274.6:c.1796-429_1796-426dup	ENSP00000398879.2:n.1796-429_1796-426dup
ENST00000440126.7:c.1892-429_1892-426dup	ENSP00000387483.2:n.1892-429_1892-426dup
NM_000484.3:c.1964-429_1964-426dup	NP_000475.1:n.1964-429_1964-426dup
NM_001136016.3:c.1892-429_1892-426dup	NP_001129488.1:n.1892-429_1892-426dup
NM_001136129.2:c.1571-429_1571-426dup	NP_001129601.1:n.1571-429_1571-426dup
NM_001136130.2:c.1796-429_1796-426dup	NP_001129602.1:n.1796-429_1796-426dup
NM_001136131.2:c.1634-429_1634-426dup	NP_001129603.1:n.1634-429_1634-426dup
NM_001204301.1:c.1910-429_1910-426dup	NP_001191230.1:n.1910-429_1910-426dup
NM_001204302.1:c.1853-429_1853-426dup	NP_001191231.1:n.1853-429_1853-426dup
NM_001204303.1:c.1685-429_1685-426dup	NP_001191232.1:n.1685-429_1685-426dup
NM_201413.2:c.1907-429_1907-426dup	NP_958816.1:n.1907-429_1907-426dup
NM_201414.2:c.1739-429_1739-426dup	NP_958817.1:n.1739-429_1739-426dup
NM_000484.4:c.1964-429_1964-426dup MANE Select	NP_000475.1:n.1964-429_1964-426dup
NM_001136129.3:c.1571-429_1571-426dup	NP_001129601.1:n.1571-429_1571-426dup
NM_001136130.3:c.1796-429_1796-426dup	NP_001129602.1:n.1796-429_1796-426dup
NM_001204301.2:c.1910-429_1910-426dup	NP_001191230.1:n.1910-429_1910-426dup
NM_001204302.2:c.1853-429_1853-426dup	NP_001191231.1:n.1853-429_1853-426dup
NM_001204303.2:c.1685-429_1685-426dup	NP_001191232.1:n.1685-429_1685-426dup
NM_201413.3:c.1907-429_1907-426dup	NP_958816.1:n.1907-429_1907-426dup
NM_201414.3:c.1739-429_1739-426dup	NP_958817.1:n.1739-429_1739-426dup
NM_001136131.3:c.1634-429_1634-426dup	NP_001129603.1:n.1634-429_1634-426dup
NM_001385253.1:c.1796-429_1796-426dup	NP_001372182.1:n.1796-429_1796-426dup