Canonical Allele Identifier: CA390304758
Gene: PSEN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73206403G>A , CM000676.2:g.73206403G>A GRCh38
NC_000014.8:g.73673111G>A , CM000676.1:g.73673111G>A GRCh37
NC_000014.7:g.72742864G>A NCBI36
NG_007386.2:g.74933G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553599.6:c.874G>A ENSP00000452477.2:p.Val292Met
ENST00000554131.6:c.886G>A ENSP00000451915.2:p.Val296Met
ENST00000554995.2:n.1636G>A
ENST00000555386.6:c.874G>A ENSP00000450845.1:p.Val292Met
ENST00000556066.2:n.1312G>A
ENST00000556951.6:c.874G>A ENSP00000450551.2:p.Val292Met
ENST00000557293.6:c.766G>A ENSP00000451880.2:p.Val256Met
ENST00000559361.6:c.*830G>A ENSP00000454156.1:n.*830G>A
ENST00000697912.1:c.874G>A ENSP00000513477.1:p.Val292Met
ENST00000697913.1:n.1140G>A
ENST00000700265.1:c.874G>A ENSP00000514901.1:p.Val292Met
ENST00000700266.1:c.*1098G>A ENSP00000514902.1:n.*1098G>A
ENST00000700267.1:c.886G>A ENSP00000514903.1:p.Val296Met
ENST00000700268.1:c.886G>A ENSP00000514904.1:p.Val296Met
ENST00000700269.1:c.886G>A ENSP00000514905.1:p.Val296Met
ENST00000700270.1:n.1142G>A
ENST00000700271.1:c.874G>A ENSP00000514906.1:p.Val292Met
ENST00000700272.1:c.*830G>A ENSP00000514907.1:n.*830G>A
ENST00000700273.1:c.874G>A ENSP00000514908.1:p.Val292Met
ENST00000700302.1:c.886G>A ENSP00000514929.1:p.Val296Met
ENST00000700303.1:c.*548G>A ENSP00000514930.1:n.*548G>A
ENST00000700304.1:c.*830G>A ENSP00000514931.1:n.*830G>A
ENST00000700305.1:c.*444G>A ENSP00000514932.1:n.*444G>A
ENST00000700306.1:c.886G>A ENSP00000514933.1:p.Val296Met
ENST00000700307.1:c.787G>A ENSP00000514934.1:p.Val263Met
ENST00000700308.1:c.*830G>A ENSP00000514935.1:n.*830G>A
ENST00000700309.1:c.*975G>A ENSP00000514936.1:n.*975G>A
ENST00000700310.1:c.775G>A ENSP00000514937.1:p.Val259Met
ENST00000700311.1:c.886G>A ENSP00000514938.1:p.Val296Met
ENST00000700312.1:c.637G>A ENSP00000514939.1:p.Val213Met
ENST00000700313.1:c.874G>A ENSP00000514940.1:p.Val292Met
ENST00000700314.1:c.*825G>A ENSP00000514941.1:n.*825G>A
ENST00000700315.1:c.*444G>A ENSP00000514942.1:n.*444G>A
ENST00000700316.1:c.*666G>A ENSP00000514943.1:n.*666G>A
ENST00000700317.1:c.886G>A ENSP00000514944.1:p.Val296Met
ENST00000700318.1:c.*548G>A ENSP00000514945.1:n.*548G>A
ENST00000700319.1:c.*326G>A ENSP00000514946.1:n.*326G>A
ENST00000700320.1:c.913G>A ENSP00000514947.1:p.Val305Met
ENST00000700321.1:c.886G>A ENSP00000514948.1:p.Val296Met
ENST00000700322.1:c.874G>A ENSP00000514949.1:p.Val292Met
ENST00000700323.1:c.886G>A ENSP00000514950.1:p.Val296Met
ENST00000700324.1:c.874G>A ENSP00000514951.1:p.Val292Met
ENST00000700375.1:c.886G>A ENSP00000514966.1:p.Val296Met
ENST00000700377.1:c.*354G>A ENSP00000514967.1:n.*354G>A
ENST00000700378.1:c.886G>A ENSP00000514968.1:p.Val296Met
ENST00000700379.1:n.1284G>A
ENST00000700389.1:c.874G>A ENSP00000514970.1:p.Val292Met
ENST00000700390.1:n.2597G>A
ENST00000700391.1:n.97G>A
ENST00000700404.1:n.1885G>A
ENST00000700433.1:n.1137G>A
ENST00000700434.1:n.1139G>A
ENST00000700435.1:n.1021G>A
ENST00000700436.1:c.886G>A ENSP00000514987.1:p.Val296Met
ENST00000700437.1:c.637G>A ENSP00000514988.1:p.Val213Met
ENST00000700467.1:n.1143G>A
ENST00000700468.1:c.775G>A ENSP00000515001.1:p.Val259Met
ENST00000700469.1:c.874G>A ENSP00000515002.1:p.Val292Met
ENST00000324501.10:c.886G>A MANE Select ENSP00000326366.5:p.Val296Met
ENST00000324501.9:c.886G>A ENSP00000326366.5:p.Val296Met
ENST00000357710.8:c.874G>A ENSP00000350342.4:p.Val292Met
ENST00000394164.5:c.874G>A ENSP00000377719.1:p.Val292Met
ENST00000406768.1:c.610G>A ENSP00000385948.1:p.Val204Met
ENST00000553855.5:c.886G>A ENSP00000452242.1:p.Val296Met
ENST00000554995.1:n.438G>A
ENST00000555386.5:c.874G>A ENSP00000450845.1:p.Val292Met
ENST00000555867.1:n.251G>A
ENST00000557511.5:c.886G>A ENSP00000451429.1:p.Val296Met
NM_000021.3:c.886G>A NP_000012.1:p.Val296Met
NM_007318.2:c.874G>A NP_015557.2:p.Val292Met
XM_005267864.1:c.886G>A XP_005267921.1:p.Val296Met
XM_005267866.1:c.874G>A XP_005267923.1:p.Val292Met
XM_011536971.1:c.886G>A XP_011535273.1:p.Val296Met
XM_011536972.1:c.886G>A XP_011535274.1:p.Val296Met
XM_011536973.1:c.874G>A XP_011535275.1:p.Val292Met
XM_011536974.1:c.874G>A XP_011535276.1:p.Val292Met
XM_005267864.3:c.886G>A XP_005267921.1:p.Val296Met
XM_005267866.2:c.874G>A XP_005267923.1:p.Val292Met
XM_011536972.2:c.886G>A XP_011535274.1:p.Val296Met
XM_011536973.2:c.874G>A XP_011535275.1:p.Val292Met
XM_011536974.2:c.874G>A XP_011535276.1:p.Val292Met
NM_000021.4:c.886G>A MANE Select NP_000012.1:p.Val296Met
NM_007318.3:c.874G>A NP_015557.2:p.Val292Met