Canonical Allele Identifier: CA262618874
Gene: PSEN1 HGNC NCBI

Linked Data

dbSNP Id: rs767531472

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73212130_73212140del , CM000676.2:g.73212130_73212140del GRCh38
NC_000014.8:g.73678838_73678848del , CM000676.1:g.73678838_73678848del GRCh37
NC_000014.7:g.72748591_72748601del NCBI36
NG_007386.2:g.80660_80670del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553599.6:c.1117+188_1117+198del ENSP00000452477.2:n.1117+188_1117+198del
ENST00000554131.6:c.1129+188_1129+198del ENSP00000451915.2:n.1129+188_1129+198del
ENST00000554995.2:n.1879+188_1879+198del
ENST00000555386.6:c.*84+188_*84+198del ENSP00000450845.1:n.*84+188_*84+198del
ENST00000556066.2:n.1555+188_1555+198del
ENST00000556951.6:c.1117+188_1117+198del ENSP00000450551.2:n.1117+188_1117+198del
ENST00000557293.6:c.1009+188_1009+198del ENSP00000451880.2:n.1009+188_1009+198del
ENST00000559361.6:c.*1073+188_*1073+198del ENSP00000454156.1:n.*1073+188_*1073+198del
ENST00000697912.1:c.1117+188_1117+198del ENSP00000513477.1:n.1117+188_1117+198del
ENST00000697913.1:n.6679+188_6679+198del
ENST00000700265.1:c.1117+188_1117+198del ENSP00000514901.1:n.1117+188_1117+198del
ENST00000700266.1:c.*1341+188_*1341+198del ENSP00000514902.1:n.*1341+188_*1341+198del
ENST00000700267.1:c.1129+188_1129+198del ENSP00000514903.1:n.1129+188_1129+198del
ENST00000700268.1:c.1129+188_1129+198del ENSP00000514904.1:n.1129+188_1129+198del
ENST00000700269.1:c.1129+188_1129+198del ENSP00000514905.1:n.1129+188_1129+198del
ENST00000700271.1:c.944-4996_944-4986del ENSP00000514906.1:n.944-4996_944-4986del
ENST00000700272.1:c.*1073+188_*1073+198del ENSP00000514907.1:n.*1073+188_*1073+198del
ENST00000700273.1:c.1117+188_1117+198del ENSP00000514908.1:n.1117+188_1117+198del
ENST00000700302.1:c.1172+145_1172+155del ENSP00000514929.1:n.1172+145_1172+155del
ENST00000700303.1:c.*791+188_*791+198del ENSP00000514930.1:n.*791+188_*791+198del
ENST00000700304.1:c.*1073+188_*1073+198del ENSP00000514931.1:n.*1073+188_*1073+198del
ENST00000700305.1:c.*687+188_*687+198del ENSP00000514932.1:n.*687+188_*687+198del
ENST00000700306.1:c.1129+188_1129+198del ENSP00000514933.1:n.1129+188_1129+198del
ENST00000700307.1:c.1030+188_1030+198del ENSP00000514934.1:n.1030+188_1030+198del
ENST00000700308.1:c.*1073+188_*1073+198del ENSP00000514935.1:n.*1073+188_*1073+198del
ENST00000700309.1:c.*1218+188_*1218+198del ENSP00000514936.1:n.*1218+188_*1218+198del
ENST00000700310.1:c.*84+188_*84+198del ENSP00000514937.1:n.*84+188_*84+198del
ENST00000700311.1:c.1172+145_1172+155del ENSP00000514938.1:n.1172+145_1172+155del
ENST00000700312.1:c.880+188_880+198del ENSP00000514939.1:n.880+188_880+198del
ENST00000700313.1:c.1117+188_1117+198del ENSP00000514940.1:n.1117+188_1117+198del
ENST00000700314.1:c.*1068+188_*1068+198del ENSP00000514941.1:n.*1068+188_*1068+198del
ENST00000700315.1:c.*687+188_*687+198del ENSP00000514942.1:n.*687+188_*687+198del
ENST00000700316.1:c.*909+188_*909+198del ENSP00000514943.1:n.*909+188_*909+198del
ENST00000700317.1:c.1129+188_1129+198del ENSP00000514944.1:n.1129+188_1129+198del
ENST00000700318.1:c.*791+188_*791+198del ENSP00000514945.1:n.*791+188_*791+198del
ENST00000700319.1:c.*569+188_*569+198del ENSP00000514946.1:n.*569+188_*569+198del
ENST00000700320.1:c.1156+188_1156+198del ENSP00000514947.1:n.1156+188_1156+198del
ENST00000700321.1:c.1129+188_1129+198del ENSP00000514948.1:n.1129+188_1129+198del
ENST00000700322.1:c.1117+188_1117+198del ENSP00000514949.1:n.1117+188_1117+198del
ENST00000700323.1:c.1129+188_1129+198del ENSP00000514950.1:n.1129+188_1129+198del
ENST00000700324.1:c.1117+188_1117+198del ENSP00000514951.1:n.1117+188_1117+198del
ENST00000700375.1:c.1129+188_1129+198del ENSP00000514966.1:n.1129+188_1129+198del
ENST00000700377.1:c.*597+188_*597+198del ENSP00000514967.1:n.*597+188_*597+198del
ENST00000700378.1:c.1129+188_1129+198del ENSP00000514968.1:n.1129+188_1129+198del
ENST00000700379.1:n.1527+188_1527+198del
ENST00000700389.1:c.1117+188_1117+198del ENSP00000514970.1:n.1117+188_1117+198del
ENST00000700390.1:n.2840+188_2840+198del
ENST00000700391.1:n.340+188_340+198del
ENST00000700404.1:n.2128+188_2128+198del
ENST00000700435.1:n.1264+188_1264+198del
ENST00000700436.1:c.*84+188_*84+198del ENSP00000514987.1:n.*84+188_*84+198del
ENST00000700437.1:c.880+188_880+198del ENSP00000514988.1:n.880+188_880+198del
ENST00000700468.1:c.1018+188_1018+198del ENSP00000515001.1:n.1018+188_1018+198del
ENST00000700469.1:c.1117+188_1117+198del ENSP00000515002.1:n.1117+188_1117+198del
ENST00000324501.10:c.1129+188_1129+198del MANE Select ENSP00000326366.5:n.1129+188_1129+198del
ENST00000324501.9:c.1129+188_1129+198del ENSP00000326366.5:n.1129+188_1129+198del
ENST00000357710.8:c.1117+188_1117+198del ENSP00000350342.4:n.1117+188_1117+198del
ENST00000394164.5:c.1117+188_1117+198del ENSP00000377719.1:n.1117+188_1117+198del
ENST00000406768.1:c.853+188_853+198del ENSP00000385948.1:n.853+188_853+198del
ENST00000553855.5:c.1221+188_1221+198del ENSP00000452242.1:n.1221+188_1221+198del
ENST00000555386.5:c.1209+188_1209+198del ENSP00000450845.1:n.1209+188_1209+198del
ENST00000555867.1:n.494+188_494+198del
ENST00000557511.5:c.956-4996_956-4986del ENSP00000451429.1:n.956-4996_956-4986del
NM_000021.3:c.1129+188_1129+198del NP_000012.1:n.1129+188_1129+198del
NM_007318.2:c.1117+188_1117+198del NP_015557.2:n.1117+188_1117+198del
XM_005267864.1:c.1129+188_1129+198del XP_005267921.1:n.1129+188_1129+198del
XM_005267866.1:c.1117+188_1117+198del XP_005267923.1:n.1117+188_1117+198del
XM_011536971.1:c.1129+188_1129+198del XP_011535273.1:n.1129+188_1129+198del
XM_011536972.1:c.1129+188_1129+198del XP_011535274.1:n.1129+188_1129+198del
XM_011536973.1:c.1117+188_1117+198del XP_011535275.1:n.1117+188_1117+198del
XM_011536974.1:c.1117+188_1117+198del XP_011535276.1:n.1117+188_1117+198del
XM_005267864.3:c.1129+188_1129+198del XP_005267921.1:n.1129+188_1129+198del
XM_005267866.2:c.1117+188_1117+198del XP_005267923.1:n.1117+188_1117+198del
XM_011536972.2:c.1129+188_1129+198del XP_011535274.1:n.1129+188_1129+198del
XM_011536973.2:c.1117+188_1117+198del XP_011535275.1:n.1117+188_1117+198del
XM_011536974.2:c.1117+188_1117+198del XP_011535276.1:n.1117+188_1117+198del
NM_000021.4:c.1129+188_1129+198del MANE Select NP_000012.1:n.1129+188_1129+198del
NM_007318.3:c.1117+188_1117+198del NP_015557.2:n.1117+188_1117+198del