Canonical Allele Identifier: CA2383554960
Gene: APP HGNC NCBI

Linked Data

dbSNP Id: rs2038167534

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897677_25897678insGCTAGAA , CM000683.2:g.25897677_25897678insGCTAGAA GRCh38
NC_000021.8:g.27269989_27269990insGCTAGAA , CM000683.1:g.27269989_27269990insGCTAGAA GRCh37
NC_000021.7:g.26191860_26191861insGCTAGAA NCBI36
NG_007376.1:g.278143_278144insTTCTAGC
NG_007376.2:g.278451_278452insTTCTAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.1931-5_1931-4insTTCTAGC
ENST00000707133.1:n.361-5_361-4insTTCTAGC
ENST00000707134.1:n.630-5_630-4insTTCTAGC
ENST00000346798.8:c.1964-5_1964-4insTTCTAGC MANE Select ENSP00000284981.4:n.1964-5_1964-4insTTCTA...
ENST00000346798.7:c.1964-5_1964-4insTTCTAGC ENSP00000284981.4:n.1964-5_1964-4insTTCTA...
ENST00000348990.9:c.1739-5_1739-4insTTCTAGC ENSP00000345463.5:n.1739-5_1739-4insTTCTA...
ENST00000354192.7:c.1571-5_1571-4insTTCTAGC ENSP00000346129.3:n.1571-5_1571-4insTTCTA...
ENST00000357903.7:c.1907-5_1907-4insTTCTAGC ENSP00000350578.3:n.1907-5_1907-4insTTCTA...
ENST00000358918.7:c.1910-5_1910-4insTTCTAGC ENSP00000351796.3:n.1910-5_1910-4insTTCTA...
ENST00000359726.7:c.1634-5_1634-4insTTCTAGC ENSP00000352760.4:n.1634-5_1634-4insTTCTA...
ENST00000439274.6:c.1796-5_1796-4insTTCTAGC ENSP00000398879.2:n.1796-5_1796-4insTTCTA...
ENST00000440126.7:c.1892-5_1892-4insTTCTAGC ENSP00000387483.2:n.1892-5_1892-4insTTCTA...
ENST00000464867.1:n.306_307insTTCTAGC
NM_000484.3:c.1964-5_1964-4insTTCTAGC NP_000475.1:n.1964-5_1964-4insTTCTAGC
NM_001136016.3:c.1892-5_1892-4insTTCTAGC NP_001129488.1:n.1892-5_1892-4insTTCTAGC
NM_001136129.2:c.1571-5_1571-4insTTCTAGC NP_001129601.1:n.1571-5_1571-4insTTCTAGC
NM_001136130.2:c.1796-5_1796-4insTTCTAGC NP_001129602.1:n.1796-5_1796-4insTTCTAGC
NM_001136131.2:c.1634-5_1634-4insTTCTAGC NP_001129603.1:n.1634-5_1634-4insTTCTAGC
NM_001204301.1:c.1910-5_1910-4insTTCTAGC NP_001191230.1:n.1910-5_1910-4insTTCTAGC
NM_001204302.1:c.1853-5_1853-4insTTCTAGC NP_001191231.1:n.1853-5_1853-4insTTCTAGC
NM_001204303.1:c.1685-5_1685-4insTTCTAGC NP_001191232.1:n.1685-5_1685-4insTTCTAGC
NM_201413.2:c.1907-5_1907-4insTTCTAGC NP_958816.1:n.1907-5_1907-4insTTCTAGC
NM_201414.2:c.1739-5_1739-4insTTCTAGC NP_958817.1:n.1739-5_1739-4insTTCTAGC
NM_000484.4:c.1964-5_1964-4insTTCTAGC MANE Select NP_000475.1:n.1964-5_1964-4insTTCTAGC
NM_001136129.3:c.1571-5_1571-4insTTCTAGC NP_001129601.1:n.1571-5_1571-4insTTCTAGC
NM_001136130.3:c.1796-5_1796-4insTTCTAGC NP_001129602.1:n.1796-5_1796-4insTTCTAGC
NM_001204301.2:c.1910-5_1910-4insTTCTAGC NP_001191230.1:n.1910-5_1910-4insTTCTAGC
NM_001204302.2:c.1853-5_1853-4insTTCTAGC NP_001191231.1:n.1853-5_1853-4insTTCTAGC
NM_001204303.2:c.1685-5_1685-4insTTCTAGC NP_001191232.1:n.1685-5_1685-4insTTCTAGC
NM_201413.3:c.1907-5_1907-4insTTCTAGC NP_958816.1:n.1907-5_1907-4insTTCTAGC
NM_201414.3:c.1739-5_1739-4insTTCTAGC NP_958817.1:n.1739-5_1739-4insTTCTAGC
NM_001136131.3:c.1634-5_1634-4insTTCTAGC NP_001129603.1:n.1634-5_1634-4insTTCTAGC
NM_001385253.1:c.1796-5_1796-4insTTCTAGC NP_001372182.1:n.1796-5_1796-4insTTCTAGC