Canonical Allele Identifier: CA2654122311
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25891619_25891620dup , CM000683.2:g.25891619_25891620dup GRCh38
NC_000021.8:g.27263931_27263932dup , CM000683.1:g.27263931_27263932dup GRCh37
NC_000021.7:g.26185802_26185803dup NCBI36
NG_007376.1:g.284201_284202dup
NG_007376.2:g.284509_284510dup

Transcript Alleles

HGVS Amino-acid change
ENST00000707132.1:n.2178+102_2178+103dup
ENST00000707133.1:n.608+102_608+103dup
ENST00000707134.1:n.877+102_877+103dup
ENST00000346798.8:c.2211+102_2211+103dup MANE Select ENSP00000284981.4:n.2211+102_2211+103dup
ENST00000346798.7:c.2211+102_2211+103dup ENSP00000284981.4:n.2211+102_2211+103dup
ENST00000348990.9:c.1986+102_1986+103dup ENSP00000345463.5:n.1986+102_1986+103dup
ENST00000354192.7:c.1818+102_1818+103dup ENSP00000346129.3:n.1818+102_1818+103dup
ENST00000357903.7:c.2154+102_2154+103dup ENSP00000350578.3:n.2154+102_2154+103dup
ENST00000358918.7:c.2157+102_2157+103dup ENSP00000351796.3:n.2157+102_2157+103dup
ENST00000359726.7:c.1881+102_1881+103dup ENSP00000352760.4:n.1881+102_1881+103dup
ENST00000439274.6:c.2043+102_2043+103dup ENSP00000398879.2:n.2043+102_2043+103dup
ENST00000440126.7:c.2139+102_2139+103dup ENSP00000387483.2:n.2139+102_2139+103dup
ENST00000464867.1:n.558+102_558+103dup
NM_000484.3:c.2211+102_2211+103dup NP_000475.1:n.2211+102_2211+103dup
NM_001136016.3:c.2139+102_2139+103dup NP_001129488.1:n.2139+102_2139+103dup
NM_001136129.2:c.1818+102_1818+103dup NP_001129601.1:n.1818+102_1818+103dup
NM_001136130.2:c.2043+102_2043+103dup NP_001129602.1:n.2043+102_2043+103dup
NM_001136131.2:c.1881+102_1881+103dup NP_001129603.1:n.1881+102_1881+103dup
NM_001204301.1:c.2157+102_2157+103dup NP_001191230.1:n.2157+102_2157+103dup
NM_001204302.1:c.2100+102_2100+103dup NP_001191231.1:n.2100+102_2100+103dup
NM_001204303.1:c.1932+102_1932+103dup NP_001191232.1:n.1932+102_1932+103dup
NM_201413.2:c.2154+102_2154+103dup NP_958816.1:n.2154+102_2154+103dup
NM_201414.2:c.1986+102_1986+103dup NP_958817.1:n.1986+102_1986+103dup
NM_000484.4:c.2211+102_2211+103dup MANE Select NP_000475.1:n.2211+102_2211+103dup
NM_001136129.3:c.1818+102_1818+103dup NP_001129601.1:n.1818+102_1818+103dup
NM_001136130.3:c.2043+102_2043+103dup NP_001129602.1:n.2043+102_2043+103dup
NM_001204301.2:c.2157+102_2157+103dup NP_001191230.1:n.2157+102_2157+103dup
NM_001204302.2:c.2100+102_2100+103dup NP_001191231.1:n.2100+102_2100+103dup
NM_001204303.2:c.1932+102_1932+103dup NP_001191232.1:n.1932+102_1932+103dup
NM_201413.3:c.2154+102_2154+103dup NP_958816.1:n.2154+102_2154+103dup
NM_201414.3:c.1986+102_1986+103dup NP_958817.1:n.1986+102_1986+103dup
NM_001136131.3:c.1881+102_1881+103dup NP_001129603.1:n.1881+102_1881+103dup
NM_001385253.1:c.2043+102_2043+103dup NP_001372182.1:n.2043+102_2043+103dup