Canonical Allele Identifier: CA390295960

Gene: PSEN1

Linked Data

• MyVariant Identifiers: chr14:g.73653574G>A (hg19) ; chr14:g.73186866G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73186866G>A , CM000676.2:g.73186866G>A	GRCh38
NC_000014.8:g.73653574G>A , CM000676.1:g.73653574G>A	GRCh37
NC_000014.7:g.72723327G>A	NCBI36
NG_007386.2:g.55396G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553599.6:c.482G>A	ENSP00000452477.2:p.Trp161Ter
ENST00000554131.6:c.494G>A	ENSP00000451915.2:p.Trp165Ter
ENST00000555386.6:c.482G>A	ENSP00000450845.1:p.Trp161Ter
ENST00000556066.2:n.920G>A
ENST00000556951.6:c.482G>A	ENSP00000450551.2:p.Trp161Ter
ENST00000557293.6:c.494G>A	ENSP00000451880.2:p.Trp165Ter
ENST00000559361.6:c.*438G>A	ENSP00000454156.1:n.*438G>A
ENST00000697912.1:c.482G>A	ENSP00000513477.1:p.Trp161Ter
ENST00000697913.1:n.748G>A
ENST00000700265.1:c.482G>A	ENSP00000514901.1:p.Trp161Ter
ENST00000700266.1:c.*706G>A	ENSP00000514902.1:n.*706G>A
ENST00000700267.1:c.494G>A	ENSP00000514903.1:p.Trp165Ter
ENST00000700268.1:c.494G>A	ENSP00000514904.1:p.Trp165Ter
ENST00000700269.1:c.494G>A	ENSP00000514905.1:p.Trp165Ter
ENST00000700270.1:n.750G>A
ENST00000700271.1:c.482G>A	ENSP00000514906.1:p.Trp161Ter
ENST00000700272.1:c.*438G>A	ENSP00000514907.1:n.*438G>A
ENST00000700273.1:c.482G>A	ENSP00000514908.1:p.Trp161Ter
ENST00000700302.1:c.494G>A	ENSP00000514929.1:p.Trp165Ter
ENST00000700303.1:c.*156G>A	ENSP00000514930.1:n.*156G>A
ENST00000700304.1:c.*438G>A	ENSP00000514931.1:n.*438G>A
ENST00000700305.1:c.*52G>A	ENSP00000514932.1:n.*52G>A
ENST00000700306.1:c.494G>A	ENSP00000514933.1:p.Trp165Ter
ENST00000700307.1:c.494G>A	ENSP00000514934.1:p.Trp165Ter
ENST00000700308.1:c.*438G>A	ENSP00000514935.1:n.*438G>A
ENST00000700309.1:c.*583G>A	ENSP00000514936.1:n.*583G>A
ENST00000700310.1:c.482G>A	ENSP00000514937.1:p.Trp161Ter
ENST00000700311.1:c.494G>A	ENSP00000514938.1:p.Trp165Ter
ENST00000700312.1:c.245G>A	ENSP00000514939.1:p.Trp82Ter
ENST00000700313.1:c.482G>A	ENSP00000514940.1:p.Trp161Ter
ENST00000700314.1:c.*433G>A	ENSP00000514941.1:n.*433G>A
ENST00000700315.1:c.*52G>A	ENSP00000514942.1:n.*52G>A
ENST00000700316.1:c.*274G>A	ENSP00000514943.1:n.*274G>A
ENST00000700317.1:c.494G>A	ENSP00000514944.1:p.Trp165Ter
ENST00000700318.1:c.*156G>A	ENSP00000514945.1:n.*156G>A
ENST00000700319.1:c.481-5778G>A	ENSP00000514946.1:n.481-5778G>A
ENST00000700320.1:c.494G>A	ENSP00000514947.1:p.Trp165Ter
ENST00000700321.1:c.494G>A	ENSP00000514948.1:p.Trp165Ter
ENST00000700322.1:c.482G>A	ENSP00000514949.1:p.Trp161Ter
ENST00000700323.1:c.494G>A	ENSP00000514950.1:p.Trp165Ter
ENST00000700324.1:c.482G>A	ENSP00000514951.1:p.Trp161Ter
ENST00000700375.1:c.494G>A	ENSP00000514966.1:p.Trp165Ter
ENST00000700376.1:n.1078G>A
ENST00000700377.1:c.494G>A	ENSP00000514967.1:p.Trp165Ter
ENST00000700378.1:c.494G>A	ENSP00000514968.1:p.Trp165Ter
ENST00000700379.1:n.892G>A
ENST00000700388.1:n.741G>A
ENST00000700389.1:c.482G>A	ENSP00000514970.1:p.Trp161Ter
ENST00000700390.1:n.2205G>A
ENST00000700404.1:n.1377G>A
ENST00000700432.1:n.851G>A
ENST00000700433.1:n.629G>A
ENST00000700434.1:n.747G>A
ENST00000700435.1:n.629G>A
ENST00000700436.1:c.494G>A	ENSP00000514987.1:p.Trp165Ter
ENST00000700437.1:c.245G>A	ENSP00000514988.1:p.Trp82Ter
ENST00000700467.1:n.751G>A
ENST00000700468.1:c.482G>A	ENSP00000515001.1:p.Trp161Ter
ENST00000700469.1:c.482G>A	ENSP00000515002.1:p.Trp161Ter
ENST00000324501.10:c.494G>A MANE Select	ENSP00000326366.5:p.Trp165Ter
ENST00000324501.9:c.494G>A	ENSP00000326366.5:p.Trp165Ter
ENST00000357710.8:c.482G>A	ENSP00000350342.4:p.Trp161Ter
ENST00000394164.5:c.482G>A	ENSP00000377719.1:p.Trp161Ter
ENST00000406768.1:c.218G>A	ENSP00000385948.1:p.Trp73Ter
ENST00000553855.5:c.494G>A	ENSP00000452242.1:p.Trp165Ter
ENST00000555386.5:c.482G>A	ENSP00000450845.1:p.Trp161Ter
ENST00000557511.5:c.494G>A	ENSP00000451429.1:p.Trp165Ter
NM_000021.3:c.494G>A	NP_000012.1:p.Trp165Ter
NM_007318.2:c.482G>A	NP_015557.2:p.Trp161Ter
XM_005267864.1:c.494G>A	XP_005267921.1:p.Trp165Ter
XM_005267866.1:c.482G>A	XP_005267923.1:p.Trp161Ter
XM_011536971.1:c.494G>A	XP_011535273.1:p.Trp165Ter
XM_011536972.1:c.494G>A	XP_011535274.1:p.Trp165Ter
XM_011536973.1:c.482G>A	XP_011535275.1:p.Trp161Ter
XM_011536974.1:c.482G>A	XP_011535276.1:p.Trp161Ter
XM_005267864.3:c.494G>A	XP_005267921.1:p.Trp165Ter
XM_005267866.2:c.482G>A	XP_005267923.1:p.Trp161Ter
XM_011536972.2:c.494G>A	XP_011535274.1:p.Trp165Ter
XM_011536973.2:c.482G>A	XP_011535275.1:p.Trp161Ter
XM_011536974.2:c.482G>A	XP_011535276.1:p.Trp161Ter
NM_000021.4:c.494G>A MANE Select	NP_000012.1:p.Trp165Ter
NM_007318.3:c.482G>A	NP_015557.2:p.Trp161Ter