Canonical Allele Identifier: CA390306280
Gene: PSEN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73219283T>G , CM000676.2:g.73219283T>G GRCh38
NC_000014.8:g.73685991T>G , CM000676.1:g.73685991T>G GRCh37
NC_000014.7:g.72755744T>G NCBI36
NG_007386.2:g.87813T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553599.6:c.1386T>G ENSP00000452477.2:p.Tyr462Ter
ENST00000554131.6:c.1398T>G ENSP00000451915.2:p.Tyr466Ter
ENST00000554995.2:n.2148T>G
ENST00000555386.6:c.*353T>G ENSP00000450845.1:n.*353T>G
ENST00000556066.2:n.1824T>G
ENST00000556951.6:c.1386T>G ENSP00000450551.2:p.Tyr462Ter
ENST00000557293.6:c.1278T>G ENSP00000451880.2:p.Tyr426Ter
ENST00000559361.6:c.*1342T>G ENSP00000454156.1:n.*1342T>G
ENST00000697912.1:c.*586T>G ENSP00000513477.1:n.*586T>G
ENST00000697913.1:n.6948T>G
ENST00000697915.1:n.755T>G
ENST00000700265.1:c.1386T>G ENSP00000514901.1:p.Tyr462Ter
ENST00000700266.1:c.*1610T>G ENSP00000514902.1:n.*1610T>G
ENST00000700267.1:c.1398T>G ENSP00000514903.1:p.Tyr466Ter
ENST00000700268.1:c.1398T>G ENSP00000514904.1:p.Tyr466Ter
ENST00000700269.1:c.1398T>G ENSP00000514905.1:p.Tyr466Ter
ENST00000700271.1:c.1212T>G ENSP00000514906.1:p.Tyr404Ter
ENST00000700272.1:c.*1342T>G ENSP00000514907.1:n.*1342T>G
ENST00000700273.1:c.1386T>G ENSP00000514908.1:p.Tyr462Ter
ENST00000700302.1:c.*214T>G ENSP00000514929.1:n.*214T>G
ENST00000700303.1:c.*1060T>G ENSP00000514930.1:n.*1060T>G
ENST00000700304.1:c.*1342T>G ENSP00000514931.1:n.*1342T>G
ENST00000700305.1:c.*956T>G ENSP00000514932.1:n.*956T>G
ENST00000700306.1:c.1398T>G ENSP00000514933.1:p.Tyr466Ter
ENST00000700307.1:c.1299T>G ENSP00000514934.1:p.Tyr433Ter
ENST00000700308.1:c.*1342T>G ENSP00000514935.1:n.*1342T>G
ENST00000700309.1:c.*1487T>G ENSP00000514936.1:n.*1487T>G
ENST00000700310.1:c.*353T>G ENSP00000514937.1:n.*353T>G
ENST00000700311.1:c.*214T>G ENSP00000514938.1:n.*214T>G
ENST00000700312.1:c.1149T>G ENSP00000514939.1:p.Tyr383Ter
ENST00000700313.1:c.1386T>G ENSP00000514940.1:p.Tyr462Ter
ENST00000700314.1:c.*1337T>G ENSP00000514941.1:n.*1337T>G
ENST00000700315.1:c.*956T>G ENSP00000514942.1:n.*956T>G
ENST00000700316.1:c.*1178T>G ENSP00000514943.1:n.*1178T>G
ENST00000700317.1:c.1398T>G ENSP00000514944.1:p.Tyr466Ter
ENST00000700318.1:c.*1060T>G ENSP00000514945.1:n.*1060T>G
ENST00000700319.1:c.*838T>G ENSP00000514946.1:n.*838T>G
ENST00000700320.1:c.1425T>G ENSP00000514947.1:p.Tyr475Ter
ENST00000700321.1:c.1398T>G ENSP00000514948.1:p.Tyr466Ter
ENST00000700322.1:c.1386T>G ENSP00000514949.1:p.Tyr462Ter
ENST00000700323.1:c.1398T>G ENSP00000514950.1:p.Tyr466Ter
ENST00000700324.1:c.1386T>G ENSP00000514951.1:p.Tyr462Ter
ENST00000700375.1:c.1398T>G ENSP00000514966.1:p.Tyr466Ter
ENST00000700377.1:c.*866T>G ENSP00000514967.1:n.*866T>G
ENST00000700378.1:c.1398T>G ENSP00000514968.1:p.Tyr466Ter
ENST00000700379.1:n.1796T>G
ENST00000700389.1:c.1386T>G ENSP00000514970.1:p.Tyr462Ter
ENST00000700390.1:n.3109T>G
ENST00000700391.1:n.609T>G
ENST00000700404.1:n.2397T>G
ENST00000700436.1:c.*353T>G ENSP00000514987.1:n.*353T>G
ENST00000700437.1:c.1149T>G ENSP00000514988.1:p.Tyr383Ter
ENST00000700468.1:c.1287T>G ENSP00000515001.1:p.Tyr429Ter
ENST00000700469.1:c.1386T>G ENSP00000515002.1:p.Tyr462Ter
ENST00000324501.10:c.1398T>G MANE Select ENSP00000326366.5:p.Tyr466Ter
ENST00000324501.9:c.1398T>G ENSP00000326366.5:p.Tyr466Ter
ENST00000357710.8:c.1386T>G ENSP00000350342.4:p.Tyr462Ter
ENST00000394164.5:c.1386T>G ENSP00000377719.1:p.Tyr462Ter
ENST00000406768.1:c.1122T>G ENSP00000385948.1:p.Tyr374Ter
ENST00000555386.5:c.1478T>G ENSP00000450845.1:n.1478T>G
ENST00000555867.1:n.763T>G
ENST00000557511.5:c.1224T>G ENSP00000451429.1:p.Tyr408Ter
NM_000021.3:c.1398T>G NP_000012.1:p.Tyr466Ter
NM_007318.2:c.1386T>G NP_015557.2:p.Tyr462Ter
XM_005267864.1:c.1398T>G XP_005267921.1:p.Tyr466Ter
XM_005267866.1:c.1386T>G XP_005267923.1:p.Tyr462Ter
XM_011536971.1:c.1398T>G XP_011535273.1:p.Tyr466Ter
XM_011536972.1:c.1398T>G XP_011535274.1:p.Tyr466Ter
XM_011536973.1:c.1386T>G XP_011535275.1:p.Tyr462Ter
XM_011536974.1:c.1386T>G XP_011535276.1:p.Tyr462Ter
XM_005267864.3:c.1398T>G XP_005267921.1:p.Tyr466Ter
XM_005267866.2:c.1386T>G XP_005267923.1:p.Tyr462Ter
XM_011536972.2:c.1398T>G XP_011535274.1:p.Tyr466Ter
XM_011536973.2:c.1386T>G XP_011535275.1:p.Tyr462Ter
XM_011536974.2:c.1386T>G XP_011535276.1:p.Tyr462Ter
NM_000021.4:c.1398T>G MANE Select NP_000012.1:p.Tyr466Ter
NM_007318.3:c.1386T>G NP_015557.2:p.Tyr462Ter