Canonical Allele Identifier: CA2146453893
Gene: PSEN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73136507G= , CM000676.2:g.73136507G= GRCh38
NC_000014.8:g.73603215G= , CM000676.1:g.73603215G= GRCh37
NC_000014.7:g.72672968G= NCBI36
NG_007386.2:g.5037G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553447.7:c.-249G= ENSP00000514869.1:n.-249G=
ENST00000553599.6:c.-254G= ENSP00000452477.2:n.-254G=
ENST00000554131.6:c.-253G= ENSP00000451915.2:n.-253G=
ENST00000555386.6:c.-212G= ENSP00000450845.1:n.-212G=
ENST00000556011.6:c.-254G= ENSP00000451662.2:n.-254G=
ENST00000556951.6:c.-208G= ENSP00000450551.2:n.-208G=
ENST00000557293.6:c.-208G= ENSP00000451880.2:n.-208G=
ENST00000697912.1:c.-212G= ENSP00000513477.1:n.-212G=
ENST00000697913.1:n.43G=
ENST00000697914.1:n.1G=
ENST00000700265.1:c.-104+59G= ENSP00000514901.1:n.-104+59G=
ENST00000700266.1:c.-212G= ENSP00000514902.1:n.-212G=
ENST00000700267.1:c.-136+59G= ENSP00000514903.1:n.-136+59G=
ENST00000700268.1:c.-208G= ENSP00000514904.1:n.-208G=
ENST00000700269.1:c.-254G= ENSP00000514905.1:n.-254G=
ENST00000700270.1:n.57G=
ENST00000700271.1:c.-212G= ENSP00000514906.1:n.-212G=
ENST00000700272.1:c.-208G= ENSP00000514907.1:n.-208G=
ENST00000700273.1:c.-254G= ENSP00000514908.1:n.-254G=
ENST00000700302.1:c.-212G= ENSP00000514929.1:n.-212G=
ENST00000700303.1:c.-212G= ENSP00000514930.1:n.-212G=
ENST00000700304.1:c.-212G= ENSP00000514931.1:n.-212G=
ENST00000700305.1:c.-212G= ENSP00000514932.1:n.-212G=
ENST00000700306.1:c.-254G= ENSP00000514933.1:n.-254G=
ENST00000700307.1:c.-212G= ENSP00000514934.1:n.-212G=
ENST00000700308.1:c.-212G= ENSP00000514935.1:n.-212G=
ENST00000700309.1:c.-212G= ENSP00000514936.1:n.-212G=
ENST00000700310.1:c.-212G= ENSP00000514937.1:n.-212G=
ENST00000700311.1:c.-253G= ENSP00000514938.1:n.-253G=
ENST00000700312.1:c.-361G= ENSP00000514939.1:n.-361G=
ENST00000700313.1:c.-249G= ENSP00000514940.1:n.-249G=
ENST00000700314.1:c.-212G= ENSP00000514941.1:n.-212G=
ENST00000700315.1:c.-212G= ENSP00000514942.1:n.-212G=
ENST00000700316.1:c.-212G= ENSP00000514943.1:n.-212G=
ENST00000700317.1:c.-180G= ENSP00000514944.1:n.-180G=
ENST00000700318.1:c.-212G= ENSP00000514945.1:n.-212G=
ENST00000700319.1:c.-212G= ENSP00000514946.1:n.-212G=
ENST00000700320.1:c.-212G= ENSP00000514947.1:n.-212G=
ENST00000700321.1:c.-214G= ENSP00000514948.1:n.-214G=
ENST00000700374.1:n.47G=
ENST00000700388.1:n.36G=
ENST00000700389.1:c.-377G= ENSP00000514970.1:n.-377G=
ENST00000324501.10:c.-212G= MANE Select ENSP00000326366.5:n.-212G=
ENST00000324501.9:c.-212G= ENSP00000326366.5:n.-212G=
ENST00000357710.8:c.-212G= ENSP00000350342.4:n.-212G=
ENST00000394157.7:c.-212G= ENSP00000377712.3:n.-212G=
ENST00000553447.6:n.31G=
ENST00000553599.5:c.-254G= ENSP00000452477.1:n.-254G=
ENST00000553719.5:c.-208G= ENSP00000451674.1:n.-208G=
ENST00000554131.5:c.-253G= ENSP00000451915.1:n.-253G=
ENST00000555254.5:c.-236G= ENSP00000450652.1:n.-236G=
ENST00000556011.5:c.-254G= ENSP00000451662.1:n.-254G=
ENST00000556533.5:c.-201G= ENSP00000452128.1:n.-201G=
ENST00000556864.5:c.-311G= ENSP00000451588.1:n.-311G=
ENST00000556951.5:c.-208G= ENSP00000450551.1:n.-208G=
ENST00000557293.5:c.-208G= ENSP00000451880.1:n.-208G=
ENST00000557356.5:c.-136+59G= ENSP00000451498.1:n.-136+59G=
ENST00000560005.6:c.-314G= ENSP00000453466.1:n.-314G=
NM_000021.3:c.-212G= NP_000012.1:n.-212G=
NM_007318.2:c.-212G= NP_015557.2:n.-212G=
XM_005267864.1:c.-208G= XP_005267921.1:n.-208G=
XM_005267866.1:c.-208G= XP_005267923.1:n.-208G=
XM_005267864.3:c.-208G= XP_005267921.1:n.-208G=
XM_005267866.2:c.-208G= XP_005267923.1:n.-208G=
NM_000021.4:c.-212G= MANE Select NP_000012.1:n.-212G=
NM_007318.3:c.-212G= NP_015557.2:n.-212G=