Canonical Allele Identifier: CA637163760

Gene: APP

Linked Data

• dbSNP Id: rs1301303959
• gnomAD v2: 21-27270380-G-GAAAT
• gnomAD v3: 21-25898068-G-GAAAT
• gnomAD v4: 21-25898068-G-GAAAT
• MyVariant Identifiers: chr21:g.27270380_27270381insAAAT (hg19) ; chr21:g.25898068_25898069insAAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25898071_25898074dup , CM000683.2:g.25898071_25898074dup	GRCh38
NC_000021.8:g.27270383_27270386dup , CM000683.1:g.27270383_27270386dup	GRCh37
NC_000021.7:g.26192254_26192257dup	NCBI36
NG_007376.1:g.277749_277752dup
NG_007376.2:g.278057_278060dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1931-399_1931-396dup
ENST00000707133.1:n.361-399_361-396dup
ENST00000707134.1:n.630-399_630-396dup
ENST00000346798.8:c.1964-399_1964-396dup MANE Select	ENSP00000284981.4:n.1964-399_1964-396dup
ENST00000346798.7:c.1964-399_1964-396dup	ENSP00000284981.4:n.1964-399_1964-396dup
ENST00000348990.9:c.1739-399_1739-396dup	ENSP00000345463.5:n.1739-399_1739-396dup
ENST00000354192.7:c.1571-399_1571-396dup	ENSP00000346129.3:n.1571-399_1571-396dup
ENST00000357903.7:c.1907-399_1907-396dup	ENSP00000350578.3:n.1907-399_1907-396dup
ENST00000358918.7:c.1910-399_1910-396dup	ENSP00000351796.3:n.1910-399_1910-396dup
ENST00000359726.7:c.1634-399_1634-396dup	ENSP00000352760.4:n.1634-399_1634-396dup
ENST00000439274.6:c.1796-399_1796-396dup	ENSP00000398879.2:n.1796-399_1796-396dup
ENST00000440126.7:c.1892-399_1892-396dup	ENSP00000387483.2:n.1892-399_1892-396dup
NM_000484.3:c.1964-399_1964-396dup	NP_000475.1:n.1964-399_1964-396dup
NM_001136016.3:c.1892-399_1892-396dup	NP_001129488.1:n.1892-399_1892-396dup
NM_001136129.2:c.1571-399_1571-396dup	NP_001129601.1:n.1571-399_1571-396dup
NM_001136130.2:c.1796-399_1796-396dup	NP_001129602.1:n.1796-399_1796-396dup
NM_001136131.2:c.1634-399_1634-396dup	NP_001129603.1:n.1634-399_1634-396dup
NM_001204301.1:c.1910-399_1910-396dup	NP_001191230.1:n.1910-399_1910-396dup
NM_001204302.1:c.1853-399_1853-396dup	NP_001191231.1:n.1853-399_1853-396dup
NM_001204303.1:c.1685-399_1685-396dup	NP_001191232.1:n.1685-399_1685-396dup
NM_201413.2:c.1907-399_1907-396dup	NP_958816.1:n.1907-399_1907-396dup
NM_201414.2:c.1739-399_1739-396dup	NP_958817.1:n.1739-399_1739-396dup
NM_000484.4:c.1964-399_1964-396dup MANE Select	NP_000475.1:n.1964-399_1964-396dup
NM_001136129.3:c.1571-399_1571-396dup	NP_001129601.1:n.1571-399_1571-396dup
NM_001136130.3:c.1796-399_1796-396dup	NP_001129602.1:n.1796-399_1796-396dup
NM_001204301.2:c.1910-399_1910-396dup	NP_001191230.1:n.1910-399_1910-396dup
NM_001204302.2:c.1853-399_1853-396dup	NP_001191231.1:n.1853-399_1853-396dup
NM_001204303.2:c.1685-399_1685-396dup	NP_001191232.1:n.1685-399_1685-396dup
NM_201413.3:c.1907-399_1907-396dup	NP_958816.1:n.1907-399_1907-396dup
NM_201414.3:c.1739-399_1739-396dup	NP_958817.1:n.1739-399_1739-396dup
NM_001136131.3:c.1634-399_1634-396dup	NP_001129603.1:n.1634-399_1634-396dup
NM_001385253.1:c.1796-399_1796-396dup	NP_001372182.1:n.1796-399_1796-396dup