Canonical Allele Identifier: CA390305582
Gene: PSEN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73211895T>G , CM000676.2:g.73211895T>G GRCh38
NC_000014.8:g.73678603T>G , CM000676.1:g.73678603T>G GRCh37
NC_000014.7:g.72748356T>G NCBI36
NG_007386.2:g.80425T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553599.6:c.1070T>G ENSP00000452477.2:p.Val357Gly
ENST00000554131.6:c.1082T>G ENSP00000451915.2:p.Val361Gly
ENST00000554995.2:n.1832T>G
ENST00000555386.6:c.*37T>G ENSP00000450845.1:n.*37T>G
ENST00000556066.2:n.1508T>G
ENST00000556951.6:c.1070T>G ENSP00000450551.2:p.Val357Gly
ENST00000557293.6:c.962T>G ENSP00000451880.2:p.Val321Gly
ENST00000559361.6:c.*1026T>G ENSP00000454156.1:n.*1026T>G
ENST00000697912.1:c.1070T>G ENSP00000513477.1:p.Val357Gly
ENST00000697913.1:n.6632T>G
ENST00000700265.1:c.1070T>G ENSP00000514901.1:p.Val357Gly
ENST00000700266.1:c.*1294T>G ENSP00000514902.1:n.*1294T>G
ENST00000700267.1:c.1082T>G ENSP00000514903.1:p.Val361Gly
ENST00000700268.1:c.1082T>G ENSP00000514904.1:p.Val361Gly
ENST00000700269.1:c.1082T>G ENSP00000514905.1:p.Val361Gly
ENST00000700271.1:c.944-5231T>G ENSP00000514906.1:n.944-5231T>G
ENST00000700272.1:c.*1026T>G ENSP00000514907.1:n.*1026T>G
ENST00000700273.1:c.1070T>G ENSP00000514908.1:p.Val357Gly
ENST00000700302.1:c.1082T>G ENSP00000514929.1:p.Val361Gly
ENST00000700303.1:c.*744T>G ENSP00000514930.1:n.*744T>G
ENST00000700304.1:c.*1026T>G ENSP00000514931.1:n.*1026T>G
ENST00000700305.1:c.*640T>G ENSP00000514932.1:n.*640T>G
ENST00000700306.1:c.1082T>G ENSP00000514933.1:p.Val361Gly
ENST00000700307.1:c.983T>G ENSP00000514934.1:p.Val328Gly
ENST00000700308.1:c.*1026T>G ENSP00000514935.1:n.*1026T>G
ENST00000700309.1:c.*1171T>G ENSP00000514936.1:n.*1171T>G
ENST00000700310.1:c.*37T>G ENSP00000514937.1:n.*37T>G
ENST00000700311.1:c.1082T>G ENSP00000514938.1:p.Val361Gly
ENST00000700312.1:c.833T>G ENSP00000514939.1:p.Val278Gly
ENST00000700313.1:c.1070T>G ENSP00000514940.1:p.Val357Gly
ENST00000700314.1:c.*1021T>G ENSP00000514941.1:n.*1021T>G
ENST00000700315.1:c.*640T>G ENSP00000514942.1:n.*640T>G
ENST00000700316.1:c.*862T>G ENSP00000514943.1:n.*862T>G
ENST00000700317.1:c.1082T>G ENSP00000514944.1:p.Val361Gly
ENST00000700318.1:c.*744T>G ENSP00000514945.1:n.*744T>G
ENST00000700319.1:c.*522T>G ENSP00000514946.1:n.*522T>G
ENST00000700320.1:c.1109T>G ENSP00000514947.1:p.Val370Gly
ENST00000700321.1:c.1082T>G ENSP00000514948.1:p.Val361Gly
ENST00000700322.1:c.1070T>G ENSP00000514949.1:p.Val357Gly
ENST00000700323.1:c.1082T>G ENSP00000514950.1:p.Val361Gly
ENST00000700324.1:c.1070T>G ENSP00000514951.1:p.Val357Gly
ENST00000700375.1:c.1082T>G ENSP00000514966.1:p.Val361Gly
ENST00000700377.1:c.*550T>G ENSP00000514967.1:n.*550T>G
ENST00000700378.1:c.1082T>G ENSP00000514968.1:p.Val361Gly
ENST00000700379.1:n.1480T>G
ENST00000700389.1:c.1070T>G ENSP00000514970.1:p.Val357Gly
ENST00000700390.1:n.2793T>G
ENST00000700391.1:n.293T>G
ENST00000700404.1:n.2081T>G
ENST00000700435.1:n.1217T>G
ENST00000700436.1:c.*37T>G ENSP00000514987.1:n.*37T>G
ENST00000700437.1:c.833T>G ENSP00000514988.1:p.Val278Gly
ENST00000700468.1:c.971T>G ENSP00000515001.1:p.Val324Gly
ENST00000700469.1:c.1070T>G ENSP00000515002.1:p.Val357Gly
ENST00000324501.10:c.1082T>G MANE Select ENSP00000326366.5:p.Val361Gly
ENST00000324501.9:c.1082T>G ENSP00000326366.5:p.Val361Gly
ENST00000357710.8:c.1070T>G ENSP00000350342.4:p.Val357Gly
ENST00000394164.5:c.1070T>G ENSP00000377719.1:p.Val357Gly
ENST00000406768.1:c.806T>G ENSP00000385948.1:p.Val269Gly
ENST00000553855.5:c.1174T>G ENSP00000452242.1:n.1174T>G
ENST00000555386.5:c.1162T>G ENSP00000450845.1:n.1162T>G
ENST00000555867.1:n.447T>G
ENST00000557511.5:c.956-5231T>G ENSP00000451429.1:n.956-5231T>G
NM_000021.3:c.1082T>G NP_000012.1:p.Val361Gly
NM_007318.2:c.1070T>G NP_015557.2:p.Val357Gly
XM_005267864.1:c.1082T>G XP_005267921.1:p.Val361Gly
XM_005267866.1:c.1070T>G XP_005267923.1:p.Val357Gly
XM_011536971.1:c.1082T>G XP_011535273.1:p.Val361Gly
XM_011536972.1:c.1082T>G XP_011535274.1:p.Val361Gly
XM_011536973.1:c.1070T>G XP_011535275.1:p.Val357Gly
XM_011536974.1:c.1070T>G XP_011535276.1:p.Val357Gly
XM_005267864.3:c.1082T>G XP_005267921.1:p.Val361Gly
XM_005267866.2:c.1070T>G XP_005267923.1:p.Val357Gly
XM_011536972.2:c.1082T>G XP_011535274.1:p.Val361Gly
XM_011536973.2:c.1070T>G XP_011535275.1:p.Val357Gly
XM_011536974.2:c.1070T>G XP_011535276.1:p.Val357Gly
NM_000021.4:c.1082T>G MANE Select NP_000012.1:p.Val361Gly
NM_007318.3:c.1070T>G NP_015557.2:p.Val357Gly