Canonical Allele Identifier: CA390305079

Gene: PSEN1

Linked Data

• MyVariant Identifiers: chr14:g.73673180A>C (hg19) ; chr14:g.73206472A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73206472A>C , CM000676.2:g.73206472A>C	GRCh38
NC_000014.8:g.73673180A>C , CM000676.1:g.73673180A>C	GRCh37
NC_000014.7:g.72742933A>C	NCBI36
NG_007386.2:g.75002A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553599.6:c.943A>C	ENSP00000452477.2:p.Ser315Arg
ENST00000554131.6:c.955A>C	ENSP00000451915.2:p.Ser319Arg
ENST00000554995.2:n.1705A>C
ENST00000555386.6:c.943A>C	ENSP00000450845.1:p.Arg315=
ENST00000556066.2:n.1381A>C
ENST00000556951.6:c.943A>C	ENSP00000450551.2:p.Ser315Arg
ENST00000557293.6:c.835A>C	ENSP00000451880.2:p.Ser279Arg
ENST00000559361.6:c.*899A>C	ENSP00000454156.1:n.*899A>C
ENST00000697912.1:c.943A>C	ENSP00000513477.1:p.Ser315Arg
ENST00000697913.1:n.1209A>C
ENST00000700265.1:c.943A>C	ENSP00000514901.1:p.Ser315Arg
ENST00000700266.1:c.*1167A>C	ENSP00000514902.1:n.*1167A>C
ENST00000700267.1:c.955A>C	ENSP00000514903.1:p.Ser319Arg
ENST00000700268.1:c.955A>C	ENSP00000514904.1:p.Ser319Arg
ENST00000700269.1:c.955A>C	ENSP00000514905.1:p.Ser319Arg
ENST00000700270.1:n.1211A>C
ENST00000700271.1:c.943A>C	ENSP00000514906.1:p.Arg315=
ENST00000700272.1:c.*899A>C	ENSP00000514907.1:n.*899A>C
ENST00000700273.1:c.943A>C	ENSP00000514908.1:p.Ser315Arg
ENST00000700302.1:c.955A>C	ENSP00000514929.1:p.Ser319Arg
ENST00000700303.1:c.*617A>C	ENSP00000514930.1:n.*617A>C
ENST00000700304.1:c.*899A>C	ENSP00000514931.1:n.*899A>C
ENST00000700305.1:c.*513A>C	ENSP00000514932.1:n.*513A>C
ENST00000700306.1:c.955A>C	ENSP00000514933.1:p.Ser319Arg
ENST00000700307.1:c.856A>C	ENSP00000514934.1:p.Ser286Arg
ENST00000700308.1:c.*899A>C	ENSP00000514935.1:n.*899A>C
ENST00000700309.1:c.*1044A>C	ENSP00000514936.1:n.*1044A>C
ENST00000700310.1:c.844A>C	ENSP00000514937.1:p.Arg282=
ENST00000700311.1:c.955A>C	ENSP00000514938.1:p.Ser319Arg
ENST00000700312.1:c.706A>C	ENSP00000514939.1:p.Ser236Arg
ENST00000700313.1:c.943A>C	ENSP00000514940.1:p.Ser315Arg
ENST00000700314.1:c.*894A>C	ENSP00000514941.1:n.*894A>C
ENST00000700315.1:c.*513A>C	ENSP00000514942.1:n.*513A>C
ENST00000700316.1:c.*735A>C	ENSP00000514943.1:n.*735A>C
ENST00000700317.1:c.955A>C	ENSP00000514944.1:p.Ser319Arg
ENST00000700318.1:c.*617A>C	ENSP00000514945.1:n.*617A>C
ENST00000700319.1:c.*395A>C	ENSP00000514946.1:n.*395A>C
ENST00000700320.1:c.982A>C	ENSP00000514947.1:p.Ser328Arg
ENST00000700321.1:c.955A>C	ENSP00000514948.1:p.Ser319Arg
ENST00000700322.1:c.943A>C	ENSP00000514949.1:p.Ser315Arg
ENST00000700323.1:c.955A>C	ENSP00000514950.1:p.Ser319Arg
ENST00000700324.1:c.943A>C	ENSP00000514951.1:p.Ser315Arg
ENST00000700375.1:c.955A>C	ENSP00000514966.1:p.Ser319Arg
ENST00000700377.1:c.*423A>C	ENSP00000514967.1:n.*423A>C
ENST00000700378.1:c.955A>C	ENSP00000514968.1:p.Ser319Arg
ENST00000700379.1:n.1353A>C
ENST00000700389.1:c.943A>C	ENSP00000514970.1:p.Ser315Arg
ENST00000700390.1:n.2666A>C
ENST00000700391.1:n.166A>C
ENST00000700404.1:n.1954A>C
ENST00000700433.1:n.1206A>C
ENST00000700434.1:n.1208A>C
ENST00000700435.1:n.1090A>C
ENST00000700436.1:c.955A>C	ENSP00000514987.1:p.Arg319=
ENST00000700437.1:c.706A>C	ENSP00000514988.1:p.Ser236Arg
ENST00000700467.1:n.1212A>C
ENST00000700468.1:c.844A>C	ENSP00000515001.1:p.Ser282Arg
ENST00000700469.1:c.943A>C	ENSP00000515002.1:p.Ser315Arg
ENST00000324501.10:c.955A>C MANE Select	ENSP00000326366.5:p.Ser319Arg
ENST00000324501.9:c.955A>C	ENSP00000326366.5:p.Ser319Arg
ENST00000357710.8:c.943A>C	ENSP00000350342.4:p.Ser315Arg
ENST00000394164.5:c.943A>C	ENSP00000377719.1:p.Ser315Arg
ENST00000406768.1:c.679A>C	ENSP00000385948.1:p.Ser227Arg
ENST00000553855.5:c.955A>C	ENSP00000452242.1:p.Arg319=
ENST00000554995.1:n.507A>C
ENST00000555386.5:c.943A>C	ENSP00000450845.1:p.Arg315=
ENST00000555867.1:n.320A>C
ENST00000557511.5:c.955A>C	ENSP00000451429.1:p.Arg319=
NM_000021.3:c.955A>C	NP_000012.1:p.Ser319Arg
NM_007318.2:c.943A>C	NP_015557.2:p.Ser315Arg
XM_005267864.1:c.955A>C	XP_005267921.1:p.Ser319Arg
XM_005267866.1:c.943A>C	XP_005267923.1:p.Ser315Arg
XM_011536971.1:c.955A>C	XP_011535273.1:p.Ser319Arg
XM_011536972.1:c.955A>C	XP_011535274.1:p.Ser319Arg
XM_011536973.1:c.943A>C	XP_011535275.1:p.Ser315Arg
XM_011536974.1:c.943A>C	XP_011535276.1:p.Ser315Arg
XM_005267864.3:c.955A>C	XP_005267921.1:p.Ser319Arg
XM_005267866.2:c.943A>C	XP_005267923.1:p.Ser315Arg
XM_011536972.2:c.955A>C	XP_011535274.1:p.Ser319Arg
XM_011536973.2:c.943A>C	XP_011535275.1:p.Ser315Arg
XM_011536974.2:c.943A>C	XP_011535276.1:p.Ser315Arg
NM_000021.4:c.955A>C MANE Select	NP_000012.1:p.Ser319Arg
NM_007318.3:c.943A>C	NP_015557.2:p.Ser315Arg