Canonical Allele Identifier: CA487097190
Gene: PSEN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.73673098A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73206390A>G , CM000676.2:g.73206390A>G GRCh38
NC_000014.8:g.73673098A>G , CM000676.1:g.73673098A>G GRCh37
NC_000014.7:g.72742851A>G NCBI36
NG_007386.2:g.74920A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553599.6:c.861A>G ENSP00000452477.2:p.Thr287=
ENST00000554131.6:c.873A>G ENSP00000451915.2:p.Thr291=
ENST00000554995.2:n.1623A>G
ENST00000555386.6:c.861A>G ENSP00000450845.1:p.Thr287=
ENST00000556066.2:n.1299A>G
ENST00000556951.6:c.861A>G ENSP00000450551.2:p.Thr287=
ENST00000557293.6:c.753A>G ENSP00000451880.2:p.Thr251=
ENST00000559361.6:c.*817A>G ENSP00000454156.1:n.*817A>G
ENST00000697912.1:c.861A>G ENSP00000513477.1:p.Thr287=
ENST00000697913.1:n.1127A>G
ENST00000700265.1:c.861A>G ENSP00000514901.1:p.Thr287=
ENST00000700266.1:c.*1085A>G ENSP00000514902.1:n.*1085A>G
ENST00000700267.1:c.873A>G ENSP00000514903.1:p.Thr291=
ENST00000700268.1:c.873A>G ENSP00000514904.1:p.Thr291=
ENST00000700269.1:c.873A>G ENSP00000514905.1:p.Thr291=
ENST00000700270.1:n.1129A>G
ENST00000700271.1:c.861A>G ENSP00000514906.1:p.Thr287=
ENST00000700272.1:c.*817A>G ENSP00000514907.1:n.*817A>G
ENST00000700273.1:c.861A>G ENSP00000514908.1:p.Thr287=
ENST00000700302.1:c.873A>G ENSP00000514929.1:p.Thr291=
ENST00000700303.1:c.*535A>G ENSP00000514930.1:n.*535A>G
ENST00000700304.1:c.*817A>G ENSP00000514931.1:n.*817A>G
ENST00000700305.1:c.*431A>G ENSP00000514932.1:n.*431A>G
ENST00000700306.1:c.873A>G ENSP00000514933.1:p.Thr291=
ENST00000700307.1:c.774A>G ENSP00000514934.1:p.Thr258=
ENST00000700308.1:c.*817A>G ENSP00000514935.1:n.*817A>G
ENST00000700309.1:c.*962A>G ENSP00000514936.1:n.*962A>G
ENST00000700310.1:c.762A>G ENSP00000514937.1:p.Thr254=
ENST00000700311.1:c.873A>G ENSP00000514938.1:p.Thr291=
ENST00000700312.1:c.624A>G ENSP00000514939.1:p.Thr208=
ENST00000700313.1:c.861A>G ENSP00000514940.1:p.Thr287=
ENST00000700314.1:c.*812A>G ENSP00000514941.1:n.*812A>G
ENST00000700315.1:c.*431A>G ENSP00000514942.1:n.*431A>G
ENST00000700316.1:c.*653A>G ENSP00000514943.1:n.*653A>G
ENST00000700317.1:c.873A>G ENSP00000514944.1:p.Thr291=
ENST00000700318.1:c.*535A>G ENSP00000514945.1:n.*535A>G
ENST00000700319.1:c.*313A>G ENSP00000514946.1:n.*313A>G
ENST00000700320.1:c.900A>G ENSP00000514947.1:p.Thr300=
ENST00000700321.1:c.873A>G ENSP00000514948.1:p.Thr291=
ENST00000700322.1:c.861A>G ENSP00000514949.1:p.Thr287=
ENST00000700323.1:c.873A>G ENSP00000514950.1:p.Thr291=
ENST00000700324.1:c.861A>G ENSP00000514951.1:p.Thr287=
ENST00000700375.1:c.873A>G ENSP00000514966.1:p.Thr291=
ENST00000700377.1:c.*341A>G ENSP00000514967.1:n.*341A>G
ENST00000700378.1:c.873A>G ENSP00000514968.1:p.Thr291=
ENST00000700379.1:n.1271A>G
ENST00000700389.1:c.861A>G ENSP00000514970.1:p.Thr287=
ENST00000700390.1:n.2584A>G
ENST00000700391.1:n.84A>G
ENST00000700404.1:n.1872A>G
ENST00000700433.1:n.1124A>G
ENST00000700434.1:n.1126A>G
ENST00000700435.1:n.1008A>G
ENST00000700436.1:c.873A>G ENSP00000514987.1:p.Thr291=
ENST00000700437.1:c.624A>G ENSP00000514988.1:p.Thr208=
ENST00000700467.1:n.1130A>G
ENST00000700468.1:c.762A>G ENSP00000515001.1:p.Thr254=
ENST00000700469.1:c.861A>G ENSP00000515002.1:p.Thr287=
ENST00000324501.10:c.873A>G MANE Select ENSP00000326366.5:p.Thr291=
ENST00000324501.9:c.873A>G ENSP00000326366.5:p.Thr291=
ENST00000357710.8:c.861A>G ENSP00000350342.4:p.Thr287=
ENST00000394164.5:c.861A>G ENSP00000377719.1:p.Thr287=
ENST00000406768.1:c.597A>G ENSP00000385948.1:p.Thr199=
ENST00000553855.5:c.873A>G ENSP00000452242.1:p.Thr291=
ENST00000554995.1:n.425A>G
ENST00000555386.5:c.861A>G ENSP00000450845.1:p.Thr287=
ENST00000555867.1:n.238A>G
ENST00000557511.5:c.873A>G ENSP00000451429.1:p.Thr291=
NM_000021.3:c.873A>G NP_000012.1:p.Thr291=
NM_007318.2:c.861A>G NP_015557.2:p.Thr287=
XM_005267864.1:c.873A>G XP_005267921.1:p.Thr291=
XM_005267866.1:c.861A>G XP_005267923.1:p.Thr287=
XM_011536971.1:c.873A>G XP_011535273.1:p.Thr291=
XM_011536972.1:c.873A>G XP_011535274.1:p.Thr291=
XM_011536973.1:c.861A>G XP_011535275.1:p.Thr287=
XM_011536974.1:c.861A>G XP_011535276.1:p.Thr287=
XM_005267864.3:c.873A>G XP_005267921.1:p.Thr291=
XM_005267866.2:c.861A>G XP_005267923.1:p.Thr287=
XM_011536972.2:c.873A>G XP_011535274.1:p.Thr291=
XM_011536973.2:c.861A>G XP_011535275.1:p.Thr287=
XM_011536974.2:c.861A>G XP_011535276.1:p.Thr287=
NM_000021.4:c.873A>G MANE Select NP_000012.1:p.Thr291=
NM_007318.3:c.861A>G NP_015557.2:p.Thr287=