Canonical Allele Identifier: CA2383555033

Gene: APP

Linked Data

• dbSNP Id: rs2038177718

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897789_25897790del , CM000683.2:g.25897789_25897790del	GRCh38
NC_000021.8:g.27270101_27270102del , CM000683.1:g.27270101_27270102del	GRCh37
NC_000021.7:g.26191972_26191973del	NCBI36
NG_007376.1:g.278033_278034del
NG_007376.2:g.278341_278342del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1931-115_1931-114del
ENST00000707133.1:n.361-115_361-114del
ENST00000707134.1:n.630-115_630-114del
ENST00000346798.8:c.1964-115_1964-114del MANE Select	ENSP00000284981.4:n.1964-115_1964-114del
ENST00000346798.7:c.1964-115_1964-114del	ENSP00000284981.4:n.1964-115_1964-114del
ENST00000348990.9:c.1739-115_1739-114del	ENSP00000345463.5:n.1739-115_1739-114del
ENST00000354192.7:c.1571-115_1571-114del	ENSP00000346129.3:n.1571-115_1571-114del
ENST00000357903.7:c.1907-115_1907-114del	ENSP00000350578.3:n.1907-115_1907-114del
ENST00000358918.7:c.1910-115_1910-114del	ENSP00000351796.3:n.1910-115_1910-114del
ENST00000359726.7:c.1634-115_1634-114del	ENSP00000352760.4:n.1634-115_1634-114del
ENST00000439274.6:c.1796-115_1796-114del	ENSP00000398879.2:n.1796-115_1796-114del
ENST00000440126.7:c.1892-115_1892-114del	ENSP00000387483.2:n.1892-115_1892-114del
ENST00000464867.1:n.196_197del
NM_000484.3:c.1964-115_1964-114del	NP_000475.1:n.1964-115_1964-114del
NM_001136016.3:c.1892-115_1892-114del	NP_001129488.1:n.1892-115_1892-114del
NM_001136129.2:c.1571-115_1571-114del	NP_001129601.1:n.1571-115_1571-114del
NM_001136130.2:c.1796-115_1796-114del	NP_001129602.1:n.1796-115_1796-114del
NM_001136131.2:c.1634-115_1634-114del	NP_001129603.1:n.1634-115_1634-114del
NM_001204301.1:c.1910-115_1910-114del	NP_001191230.1:n.1910-115_1910-114del
NM_001204302.1:c.1853-115_1853-114del	NP_001191231.1:n.1853-115_1853-114del
NM_001204303.1:c.1685-115_1685-114del	NP_001191232.1:n.1685-115_1685-114del
NM_201413.2:c.1907-115_1907-114del	NP_958816.1:n.1907-115_1907-114del
NM_201414.2:c.1739-115_1739-114del	NP_958817.1:n.1739-115_1739-114del
NM_000484.4:c.1964-115_1964-114del MANE Select	NP_000475.1:n.1964-115_1964-114del
NM_001136129.3:c.1571-115_1571-114del	NP_001129601.1:n.1571-115_1571-114del
NM_001136130.3:c.1796-115_1796-114del	NP_001129602.1:n.1796-115_1796-114del
NM_001204301.2:c.1910-115_1910-114del	NP_001191230.1:n.1910-115_1910-114del
NM_001204302.2:c.1853-115_1853-114del	NP_001191231.1:n.1853-115_1853-114del
NM_001204303.2:c.1685-115_1685-114del	NP_001191232.1:n.1685-115_1685-114del
NM_201413.3:c.1907-115_1907-114del	NP_958816.1:n.1907-115_1907-114del
NM_201414.3:c.1739-115_1739-114del	NP_958817.1:n.1739-115_1739-114del
NM_001136131.3:c.1634-115_1634-114del	NP_001129603.1:n.1634-115_1634-114del
NM_001385253.1:c.1796-115_1796-114del	NP_001372182.1:n.1796-115_1796-114del