Canonical Allele Identifier: CA2146480507
Gene: PSEN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73198066C= , CM000676.2:g.73198066C= GRCh38
NC_000014.8:g.73664774C= , CM000676.1:g.73664774C= GRCh37
NC_000014.7:g.72734527C= NCBI36
NG_007386.2:g.66596C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553599.6:c.793C= ENSP00000452477.2:p.Arg265=
ENST00000554131.6:c.805C= ENSP00000451915.2:p.Arg269=
ENST00000554995.2:n.1555C=
ENST00000555386.6:c.793C= ENSP00000450845.1:p.Arg265=
ENST00000556066.2:n.1231C=
ENST00000556951.6:c.793C= ENSP00000450551.2:p.Arg265=
ENST00000557293.6:c.685C= ENSP00000451880.2:p.Arg229=
ENST00000559361.6:c.*749C= ENSP00000454156.1:n.*749C=
ENST00000697912.1:c.793C= ENSP00000513477.1:p.Arg265=
ENST00000697913.1:n.1059C=
ENST00000700265.1:c.793C= ENSP00000514901.1:p.Arg265=
ENST00000700266.1:c.*1017C= ENSP00000514902.1:n.*1017C=
ENST00000700267.1:c.805C= ENSP00000514903.1:p.Arg269=
ENST00000700268.1:c.805C= ENSP00000514904.1:p.Arg269=
ENST00000700269.1:c.805C= ENSP00000514905.1:p.Arg269=
ENST00000700270.1:n.1061C=
ENST00000700271.1:c.793C= ENSP00000514906.1:p.Arg265=
ENST00000700272.1:c.*749C= ENSP00000514907.1:n.*749C=
ENST00000700273.1:c.793C= ENSP00000514908.1:p.Arg265=
ENST00000700302.1:c.805C= ENSP00000514929.1:p.Arg269=
ENST00000700303.1:c.*467C= ENSP00000514930.1:n.*467C=
ENST00000700304.1:c.*749C= ENSP00000514931.1:n.*749C=
ENST00000700305.1:c.*363C= ENSP00000514932.1:n.*363C=
ENST00000700306.1:c.805C= ENSP00000514933.1:p.Arg269=
ENST00000700307.1:c.769+5202C= ENSP00000514934.1:n.769+5202C=
ENST00000700308.1:c.*749C= ENSP00000514935.1:n.*749C=
ENST00000700309.1:c.*894C= ENSP00000514936.1:n.*894C=
ENST00000700310.1:c.757+5202C= ENSP00000514937.1:n.757+5202C=
ENST00000700311.1:c.805C= ENSP00000514938.1:p.Arg269=
ENST00000700312.1:c.556C= ENSP00000514939.1:p.Arg186=
ENST00000700313.1:c.793C= ENSP00000514940.1:p.Arg265=
ENST00000700314.1:c.*744C= ENSP00000514941.1:n.*744C=
ENST00000700315.1:c.*363C= ENSP00000514942.1:n.*363C=
ENST00000700316.1:c.*585C= ENSP00000514943.1:n.*585C=
ENST00000700317.1:c.805C= ENSP00000514944.1:p.Arg269=
ENST00000700318.1:c.*467C= ENSP00000514945.1:n.*467C=
ENST00000700319.1:c.*245C= ENSP00000514946.1:n.*245C=
ENST00000700320.1:c.832C= ENSP00000514947.1:p.Arg278=
ENST00000700321.1:c.805C= ENSP00000514948.1:p.Arg269=
ENST00000700322.1:c.793C= ENSP00000514949.1:p.Arg265=
ENST00000700323.1:c.805C= ENSP00000514950.1:p.Arg269=
ENST00000700324.1:c.793C= ENSP00000514951.1:p.Arg265=
ENST00000700375.1:c.805C= ENSP00000514966.1:p.Arg269=
ENST00000700377.1:c.*273C= ENSP00000514967.1:n.*273C=
ENST00000700378.1:c.805C= ENSP00000514968.1:p.Arg269=
ENST00000700379.1:n.1203C=
ENST00000700389.1:c.793C= ENSP00000514970.1:p.Arg265=
ENST00000700390.1:n.2516C=
ENST00000700404.1:n.1804C=
ENST00000700433.1:n.1056C=
ENST00000700434.1:n.1058C=
ENST00000700435.1:n.940C=
ENST00000700436.1:c.805C= ENSP00000514987.1:p.Arg269=
ENST00000700437.1:c.556C= ENSP00000514988.1:p.Arg186=
ENST00000700467.1:n.1062C=
ENST00000700468.1:c.757+5202C= ENSP00000515001.1:n.757+5202C=
ENST00000700469.1:c.793C= ENSP00000515002.1:p.Arg265=
ENST00000324501.10:c.805C= MANE Select ENSP00000326366.5:p.Arg269=
ENST00000324501.9:c.805C= ENSP00000326366.5:p.Arg269=
ENST00000357710.8:c.793C= ENSP00000350342.4:p.Arg265=
ENST00000394164.5:c.793C= ENSP00000377719.1:p.Arg265=
ENST00000406768.1:c.529C= ENSP00000385948.1:p.Arg177=
ENST00000553855.5:c.805C= ENSP00000452242.1:p.Arg269=
ENST00000554995.1:n.357C=
ENST00000555386.5:c.793C= ENSP00000450845.1:p.Arg265=
ENST00000557511.5:c.805C= ENSP00000451429.1:p.Arg269=
NM_000021.3:c.805C= NP_000012.1:p.Arg269=
NM_007318.2:c.793C= NP_015557.2:p.Arg265=
XM_005267864.1:c.805C= XP_005267921.1:p.Arg269=
XM_005267866.1:c.793C= XP_005267923.1:p.Arg265=
XM_011536971.1:c.805C= XP_011535273.1:p.Arg269=
XM_011536972.1:c.805C= XP_011535274.1:p.Arg269=
XM_011536973.1:c.793C= XP_011535275.1:p.Arg265=
XM_011536974.1:c.793C= XP_011535276.1:p.Arg265=
XM_005267864.3:c.805C= XP_005267921.1:p.Arg269=
XM_005267866.2:c.793C= XP_005267923.1:p.Arg265=
XM_011536972.2:c.805C= XP_011535274.1:p.Arg269=
XM_011536973.2:c.793C= XP_011535275.1:p.Arg265=
XM_011536974.2:c.793C= XP_011535276.1:p.Arg265=
NM_000021.4:c.805C= MANE Select NP_000012.1:p.Arg269=
NM_007318.3:c.793C= NP_015557.2:p.Arg265=