Canonical Allele Identifier: CA225090

Gene: PSEN1

Linked Data

• ClinVar Variation Id: 98065
• ClinVar RCV Id: RCV000084352 ; RCV000763347
• dbSNP Id: rs63749836
• MyVariant Identifiers: chr14:g.73659494G>A (hg19) ; chr14:g.73192786G>A (hg38)
• PubMed: PMID:8634712 ; PMID:10327206 ; PMID:10441572 ; PMID:11524469 ; PMID:14743455

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73192786G>A , CM000676.2:g.73192786G>A	GRCh38
NC_000014.8:g.73659494G>A , CM000676.1:g.73659494G>A	GRCh37
NC_000014.7:g.72729247G>A	NCBI36
NG_007386.2:g.61316G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553599.6:c.679G>A	ENSP00000452477.2:p.Ala227Thr
ENST00000554131.6:c.691G>A	ENSP00000451915.2:p.Ala231Thr
ENST00000555386.6:c.679G>A	ENSP00000450845.1:p.Ala227Thr
ENST00000556066.2:n.1117G>A
ENST00000556951.6:c.679G>A	ENSP00000450551.2:p.Ala227Thr
ENST00000557293.6:c.649+42G>A	ENSP00000451880.2:n.649+42G>A
ENST00000559361.6:c.*635G>A	ENSP00000454156.1:n.*635G>A
ENST00000697912.1:c.679G>A	ENSP00000513477.1:p.Ala227Thr
ENST00000697913.1:n.945G>A
ENST00000700265.1:c.679G>A	ENSP00000514901.1:p.Ala227Thr
ENST00000700266.1:c.*903G>A	ENSP00000514902.1:n.*903G>A
ENST00000700267.1:c.691G>A	ENSP00000514903.1:p.Ala231Thr
ENST00000700268.1:c.691G>A	ENSP00000514904.1:p.Ala231Thr
ENST00000700269.1:c.691G>A	ENSP00000514905.1:p.Ala231Thr
ENST00000700270.1:n.947G>A
ENST00000700271.1:c.679G>A	ENSP00000514906.1:p.Ala227Thr
ENST00000700272.1:c.*635G>A	ENSP00000514907.1:n.*635G>A
ENST00000700273.1:c.679G>A	ENSP00000514908.1:p.Ala227Thr
ENST00000700302.1:c.691G>A	ENSP00000514929.1:p.Ala231Thr
ENST00000700303.1:c.*353G>A	ENSP00000514930.1:n.*353G>A
ENST00000700304.1:c.*635G>A	ENSP00000514931.1:n.*635G>A
ENST00000700305.1:c.*249G>A	ENSP00000514932.1:n.*249G>A
ENST00000700306.1:c.691G>A	ENSP00000514933.1:p.Ala231Thr
ENST00000700307.1:c.691G>A	ENSP00000514934.1:p.Ala231Thr
ENST00000700308.1:c.*635G>A	ENSP00000514935.1:n.*635G>A
ENST00000700309.1:c.*780G>A	ENSP00000514936.1:n.*780G>A
ENST00000700310.1:c.679G>A	ENSP00000514937.1:p.Ala227Thr
ENST00000700311.1:c.691G>A	ENSP00000514938.1:p.Ala231Thr
ENST00000700312.1:c.442G>A	ENSP00000514939.1:p.Ala148Thr
ENST00000700313.1:c.679G>A	ENSP00000514940.1:p.Ala227Thr
ENST00000700314.1:c.*630G>A	ENSP00000514941.1:n.*630G>A
ENST00000700315.1:c.*249G>A	ENSP00000514942.1:n.*249G>A
ENST00000700316.1:c.*471G>A	ENSP00000514943.1:n.*471G>A
ENST00000700317.1:c.691G>A	ENSP00000514944.1:p.Ala231Thr
ENST00000700318.1:c.*353G>A	ENSP00000514945.1:n.*353G>A
ENST00000700319.1:c.*131G>A	ENSP00000514946.1:n.*131G>A
ENST00000700320.1:c.691G>A	ENSP00000514947.1:p.Ala231Thr
ENST00000700321.1:c.691G>A	ENSP00000514948.1:p.Ala231Thr
ENST00000700322.1:c.679G>A	ENSP00000514949.1:p.Ala227Thr
ENST00000700323.1:c.691G>A	ENSP00000514950.1:p.Ala231Thr
ENST00000700324.1:c.679G>A	ENSP00000514951.1:p.Ala227Thr
ENST00000700375.1:c.691G>A	ENSP00000514966.1:p.Ala231Thr
ENST00000700376.1:n.1275G>A
ENST00000700377.1:c.*159G>A	ENSP00000514967.1:n.*159G>A
ENST00000700378.1:c.691G>A	ENSP00000514968.1:p.Ala231Thr
ENST00000700379.1:n.1089G>A
ENST00000700388.1:n.938G>A
ENST00000700389.1:c.679G>A	ENSP00000514970.1:p.Ala227Thr
ENST00000700390.1:n.2402G>A
ENST00000700404.1:n.1690G>A
ENST00000700432.1:n.1048G>A
ENST00000700433.1:n.942G>A
ENST00000700434.1:n.944G>A
ENST00000700435.1:n.826G>A
ENST00000700436.1:c.691G>A	ENSP00000514987.1:p.Ala231Thr
ENST00000700437.1:c.442G>A	ENSP00000514988.1:p.Ala148Thr
ENST00000700467.1:n.948G>A
ENST00000700468.1:c.679G>A	ENSP00000515001.1:p.Ala227Thr
ENST00000700469.1:c.679G>A	ENSP00000515002.1:p.Ala227Thr
ENST00000324501.10:c.691G>A MANE Select	ENSP00000326366.5:p.Ala231Thr
ENST00000324501.9:c.691G>A	ENSP00000326366.5:p.Ala231Thr
ENST00000357710.8:c.679G>A	ENSP00000350342.4:p.Ala227Thr
ENST00000394164.5:c.679G>A	ENSP00000377719.1:p.Ala227Thr
ENST00000406768.1:c.415G>A	ENSP00000385948.1:p.Ala139Thr
ENST00000553855.5:c.691G>A	ENSP00000452242.1:p.Ala231Thr
ENST00000555386.5:c.679G>A	ENSP00000450845.1:p.Ala227Thr
ENST00000557511.5:c.691G>A	ENSP00000451429.1:p.Ala231Thr
NM_000021.3:c.691G>A	NP_000012.1:p.Ala231Thr
NM_007318.2:c.679G>A	NP_015557.2:p.Ala227Thr
XM_005267864.1:c.691G>A	XP_005267921.1:p.Ala231Thr
XM_005267866.1:c.679G>A	XP_005267923.1:p.Ala227Thr
XM_011536971.1:c.691G>A	XP_011535273.1:p.Ala231Thr
XM_011536972.1:c.691G>A	XP_011535274.1:p.Ala231Thr
XM_011536973.1:c.679G>A	XP_011535275.1:p.Ala227Thr
XM_011536974.1:c.679G>A	XP_011535276.1:p.Ala227Thr
XM_005267864.3:c.691G>A	XP_005267921.1:p.Ala231Thr
XM_005267866.2:c.679G>A	XP_005267923.1:p.Ala227Thr
XM_011536972.2:c.691G>A	XP_011535274.1:p.Ala231Thr
XM_011536973.2:c.679G>A	XP_011535275.1:p.Ala227Thr
XM_011536974.2:c.679G>A	XP_011535276.1:p.Ala227Thr
NM_000021.4:c.691G>A MANE Select	NP_000012.1:p.Ala231Thr
NM_007318.3:c.679G>A	NP_015557.2:p.Ala227Thr