Canonical Allele Identifier: CA7256911
Gene: PSEN1 HGNC NCBI

Linked Data

dbSNP Id: rs768878052

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73211865dup , CM000676.2:g.73211865dup GRCh38
NC_000014.8:g.73678573dup , CM000676.1:g.73678573dup GRCh37
NC_000014.7:g.72748326dup NCBI36
NG_007386.2:g.80395dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000553599.6:c.1040dup ENSP00000452477.2:p.His347GlnfsTer6
ENST00000554131.6:c.1052dup ENSP00000451915.2:p.His351GlnfsTer6
ENST00000554995.2:n.1802dup
ENST00000555386.6:c.*7dup ENSP00000450845.1:n.*7dup
ENST00000556066.2:n.1478dup
ENST00000556951.6:c.1040dup ENSP00000450551.2:p.His347GlnfsTer6
ENST00000557293.6:c.932dup ENSP00000451880.2:p.His311GlnfsTer6
ENST00000559361.6:c.*996dup ENSP00000454156.1:n.*996dup
ENST00000697912.1:c.1040dup ENSP00000513477.1:p.His347GlnfsTer6
ENST00000697913.1:n.6602dup
ENST00000700265.1:c.1040dup ENSP00000514901.1:p.His347GlnfsTer6
ENST00000700266.1:c.*1264dup ENSP00000514902.1:n.*1264dup
ENST00000700267.1:c.1052dup ENSP00000514903.1:p.His351GlnfsTer6
ENST00000700268.1:c.1052dup ENSP00000514904.1:p.His351GlnfsTer6
ENST00000700269.1:c.1052dup ENSP00000514905.1:p.His351GlnfsTer6
ENST00000700271.1:c.944-5261dup ENSP00000514906.1:n.944-5261dup
ENST00000700272.1:c.*996dup ENSP00000514907.1:n.*996dup
ENST00000700273.1:c.1040dup ENSP00000514908.1:p.His347GlnfsTer6
ENST00000700302.1:c.1052dup ENSP00000514929.1:p.His351GlnfsTer6
ENST00000700303.1:c.*714dup ENSP00000514930.1:n.*714dup
ENST00000700304.1:c.*996dup ENSP00000514931.1:n.*996dup
ENST00000700305.1:c.*610dup ENSP00000514932.1:n.*610dup
ENST00000700306.1:c.1052dup ENSP00000514933.1:p.His351GlnfsTer6
ENST00000700307.1:c.953dup ENSP00000514934.1:p.His318GlnfsTer6
ENST00000700308.1:c.*996dup ENSP00000514935.1:n.*996dup
ENST00000700309.1:c.*1141dup ENSP00000514936.1:n.*1141dup
ENST00000700310.1:c.*7dup ENSP00000514937.1:n.*7dup
ENST00000700311.1:c.1052dup ENSP00000514938.1:p.His351GlnfsTer6
ENST00000700312.1:c.803dup ENSP00000514939.1:p.His268GlnfsTer6
ENST00000700313.1:c.1040dup ENSP00000514940.1:p.His347GlnfsTer6
ENST00000700314.1:c.*991dup ENSP00000514941.1:n.*991dup
ENST00000700315.1:c.*610dup ENSP00000514942.1:n.*610dup
ENST00000700316.1:c.*832dup ENSP00000514943.1:n.*832dup
ENST00000700317.1:c.1052dup ENSP00000514944.1:p.His351GlnfsTer6
ENST00000700318.1:c.*714dup ENSP00000514945.1:n.*714dup
ENST00000700319.1:c.*492dup ENSP00000514946.1:n.*492dup
ENST00000700320.1:c.1079dup ENSP00000514947.1:p.His360GlnfsTer6
ENST00000700321.1:c.1052dup ENSP00000514948.1:p.His351GlnfsTer6
ENST00000700322.1:c.1040dup ENSP00000514949.1:p.His347GlnfsTer6
ENST00000700323.1:c.1052dup ENSP00000514950.1:p.His351GlnfsTer6
ENST00000700324.1:c.1040dup ENSP00000514951.1:p.His347GlnfsTer6
ENST00000700375.1:c.1052dup ENSP00000514966.1:p.His351GlnfsTer6
ENST00000700377.1:c.*520dup ENSP00000514967.1:n.*520dup
ENST00000700378.1:c.1052dup ENSP00000514968.1:p.His351GlnfsTer6
ENST00000700379.1:n.1450dup
ENST00000700389.1:c.1040dup ENSP00000514970.1:p.His347GlnfsTer6
ENST00000700390.1:n.2763dup
ENST00000700391.1:n.263dup
ENST00000700404.1:n.2051dup
ENST00000700435.1:n.1187dup
ENST00000700436.1:c.*7dup ENSP00000514987.1:n.*7dup
ENST00000700437.1:c.803dup ENSP00000514988.1:p.His268GlnfsTer6
ENST00000700468.1:c.941dup ENSP00000515001.1:p.His314GlnfsTer6
ENST00000700469.1:c.1040dup ENSP00000515002.1:p.His347GlnfsTer6
ENST00000324501.10:c.1052dup MANE Select ENSP00000326366.5:p.His351GlnfsTer6
ENST00000324501.9:c.1052dup ENSP00000326366.5:p.His351GlnfsTer6
ENST00000357710.8:c.1040dup ENSP00000350342.4:p.His347GlnfsTer6
ENST00000394164.5:c.1040dup ENSP00000377719.1:p.His347GlnfsTer6
ENST00000406768.1:c.776dup ENSP00000385948.1:p.His259GlnfsTer6
ENST00000553855.5:c.1144dup ENSP00000452242.1:n.1144dup
ENST00000555386.5:c.1132dup ENSP00000450845.1:n.1132dup
ENST00000555867.1:n.417dup
ENST00000557511.5:c.956-5261dup ENSP00000451429.1:n.956-5261dup
NM_000021.3:c.1052dup NP_000012.1:p.His351GlnfsTer6
NM_007318.2:c.1040dup NP_015557.2:p.His347GlnfsTer6
XM_005267864.1:c.1052dup XP_005267921.1:p.His351GlnfsTer6
XM_005267866.1:c.1040dup XP_005267923.1:p.His347GlnfsTer6
XM_011536971.1:c.1052dup XP_011535273.1:p.His351GlnfsTer6
XM_011536972.1:c.1052dup XP_011535274.1:p.His351GlnfsTer6
XM_011536973.1:c.1040dup XP_011535275.1:p.His347GlnfsTer6
XM_011536974.1:c.1040dup XP_011535276.1:p.His347GlnfsTer6
XM_005267864.3:c.1052dup XP_005267921.1:p.His351GlnfsTer6
XM_005267866.2:c.1040dup XP_005267923.1:p.His347GlnfsTer6
XM_011536972.2:c.1052dup XP_011535274.1:p.His351GlnfsTer6
XM_011536973.2:c.1040dup XP_011535275.1:p.His347GlnfsTer6
XM_011536974.2:c.1040dup XP_011535276.1:p.His347GlnfsTer6
NM_000021.4:c.1052dup MANE Select NP_000012.1:p.His351GlnfsTer6
NM_007318.3:c.1040dup NP_015557.2:p.His347GlnfsTer6