Canonical Allele Identifier: CA390306132

Gene: PSEN1

Linked Data

• MyVariant Identifiers: chr14:g.73685929T>C (hg19) ; chr14:g.73219221T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73219221T>C , CM000676.2:g.73219221T>C	GRCh38
NC_000014.8:g.73685929T>C , CM000676.1:g.73685929T>C	GRCh37
NC_000014.7:g.72755682T>C	NCBI36
NG_007386.2:g.87751T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000553599.6:c.1324T>C	ENSP00000452477.2:p.Tyr442His
ENST00000554131.6:c.1336T>C	ENSP00000451915.2:p.Tyr446His
ENST00000554995.2:n.2086T>C
ENST00000555386.6:c.*291T>C	ENSP00000450845.1:n.*291T>C
ENST00000556066.2:n.1762T>C
ENST00000556951.6:c.1324T>C	ENSP00000450551.2:p.Tyr442His
ENST00000557293.6:c.1216T>C	ENSP00000451880.2:p.Tyr406His
ENST00000559361.6:c.*1280T>C	ENSP00000454156.1:n.*1280T>C
ENST00000697912.1:c.*524T>C	ENSP00000513477.1:n.*524T>C
ENST00000697913.1:n.6886T>C
ENST00000697915.1:n.693T>C
ENST00000700265.1:c.1324T>C	ENSP00000514901.1:p.Tyr442His
ENST00000700266.1:c.*1548T>C	ENSP00000514902.1:n.*1548T>C
ENST00000700267.1:c.1336T>C	ENSP00000514903.1:p.Tyr446His
ENST00000700268.1:c.1336T>C	ENSP00000514904.1:p.Tyr446His
ENST00000700269.1:c.1336T>C	ENSP00000514905.1:p.Tyr446His
ENST00000700271.1:c.1150T>C	ENSP00000514906.1:p.Tyr384His
ENST00000700272.1:c.*1280T>C	ENSP00000514907.1:n.*1280T>C
ENST00000700273.1:c.1324T>C	ENSP00000514908.1:p.Tyr442His
ENST00000700302.1:c.*152T>C	ENSP00000514929.1:n.*152T>C
ENST00000700303.1:c.*998T>C	ENSP00000514930.1:n.*998T>C
ENST00000700304.1:c.*1280T>C	ENSP00000514931.1:n.*1280T>C
ENST00000700305.1:c.*894T>C	ENSP00000514932.1:n.*894T>C
ENST00000700306.1:c.1336T>C	ENSP00000514933.1:p.Tyr446His
ENST00000700307.1:c.1237T>C	ENSP00000514934.1:p.Tyr413His
ENST00000700308.1:c.*1280T>C	ENSP00000514935.1:n.*1280T>C
ENST00000700309.1:c.*1425T>C	ENSP00000514936.1:n.*1425T>C
ENST00000700310.1:c.*291T>C	ENSP00000514937.1:n.*291T>C
ENST00000700311.1:c.*152T>C	ENSP00000514938.1:n.*152T>C
ENST00000700312.1:c.1087T>C	ENSP00000514939.1:p.Tyr363His
ENST00000700313.1:c.1324T>C	ENSP00000514940.1:p.Tyr442His
ENST00000700314.1:c.*1275T>C	ENSP00000514941.1:n.*1275T>C
ENST00000700315.1:c.*894T>C	ENSP00000514942.1:n.*894T>C
ENST00000700316.1:c.*1116T>C	ENSP00000514943.1:n.*1116T>C
ENST00000700317.1:c.1336T>C	ENSP00000514944.1:p.Tyr446His
ENST00000700318.1:c.*998T>C	ENSP00000514945.1:n.*998T>C
ENST00000700319.1:c.*776T>C	ENSP00000514946.1:n.*776T>C
ENST00000700320.1:c.1363T>C	ENSP00000514947.1:p.Tyr455His
ENST00000700321.1:c.1336T>C	ENSP00000514948.1:p.Tyr446His
ENST00000700322.1:c.1324T>C	ENSP00000514949.1:p.Tyr442His
ENST00000700323.1:c.1336T>C	ENSP00000514950.1:p.Tyr446His
ENST00000700324.1:c.1324T>C	ENSP00000514951.1:p.Tyr442His
ENST00000700375.1:c.1336T>C	ENSP00000514966.1:p.Tyr446His
ENST00000700377.1:c.*804T>C	ENSP00000514967.1:n.*804T>C
ENST00000700378.1:c.1336T>C	ENSP00000514968.1:p.Tyr446His
ENST00000700379.1:n.1734T>C
ENST00000700389.1:c.1324T>C	ENSP00000514970.1:p.Tyr442His
ENST00000700390.1:n.3047T>C
ENST00000700391.1:n.547T>C
ENST00000700404.1:n.2335T>C
ENST00000700436.1:c.*291T>C	ENSP00000514987.1:n.*291T>C
ENST00000700437.1:c.1087T>C	ENSP00000514988.1:p.Tyr363His
ENST00000700468.1:c.1225T>C	ENSP00000515001.1:p.Tyr409His
ENST00000700469.1:c.1324T>C	ENSP00000515002.1:p.Tyr442His
ENST00000324501.10:c.1336T>C MANE Select	ENSP00000326366.5:p.Tyr446His
ENST00000324501.9:c.1336T>C	ENSP00000326366.5:p.Tyr446His
ENST00000357710.8:c.1324T>C	ENSP00000350342.4:p.Tyr442His
ENST00000394164.5:c.1324T>C	ENSP00000377719.1:p.Tyr442His
ENST00000406768.1:c.1060T>C	ENSP00000385948.1:p.Tyr354His
ENST00000555386.5:c.1416T>C	ENSP00000450845.1:n.1416T>C
ENST00000555867.1:n.701T>C
ENST00000557511.5:c.1162T>C	ENSP00000451429.1:p.Tyr388His
NM_000021.3:c.1336T>C	NP_000012.1:p.Tyr446His
NM_007318.2:c.1324T>C	NP_015557.2:p.Tyr442His
XM_005267864.1:c.1336T>C	XP_005267921.1:p.Tyr446His
XM_005267866.1:c.1324T>C	XP_005267923.1:p.Tyr442His
XM_011536971.1:c.1336T>C	XP_011535273.1:p.Tyr446His
XM_011536972.1:c.1336T>C	XP_011535274.1:p.Tyr446His
XM_011536973.1:c.1324T>C	XP_011535275.1:p.Tyr442His
XM_011536974.1:c.1324T>C	XP_011535276.1:p.Tyr442His
XM_005267864.3:c.1336T>C	XP_005267921.1:p.Tyr446His
XM_005267866.2:c.1324T>C	XP_005267923.1:p.Tyr442His
XM_011536972.2:c.1336T>C	XP_011535274.1:p.Tyr446His
XM_011536973.2:c.1324T>C	XP_011535275.1:p.Tyr442His
XM_011536974.2:c.1324T>C	XP_011535276.1:p.Tyr442His
NM_000021.4:c.1336T>C MANE Select	NP_000012.1:p.Tyr446His
NM_007318.3:c.1324T>C	NP_015557.2:p.Tyr442His