Canonical Allele Identifier: CA631298667
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1198046700

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106260_1106264del , CM000681.2:g.1106260_1106264del GRCh38
NC_000019.9:g.1106259_1106263del , CM000681.1:g.1106259_1106263del GRCh37
NC_000019.8:g.1057259_1057263del NCBI36
NG_050621.1:g.7335_7339del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.606_610del ENSP00000473614.3:p.Phe202LeufsTer?
ENST00000593032.6:c.475_479del ENSP00000465828.4:p.His159SerfsTer11
ENST00000706713.1:c.489_493del ENSP00000516510.1:p.Phe163LeufsTer?
ENST00000706714.1:c.475_479del ENSP00000516511.1:p.His159SerfsTer11
ENST00000706715.1:c.111_115del ENSP00000516512.1:p.Phe37LeufsTer?
ENST00000354171.13:c.495_499del MANE Select ENSP00000346103.7:p.Phe165LeufsTer?
ENST00000589115.6:c.477-140_477-136del ENSP00000466872.3:n.477-140_477-136del
ENST00000354171.12:c.495_499del ENSP00000346103.7:p.Phe165LeufsTer?
ENST00000585480.1:c.228_232del ENSP00000467900.1:p.Phe76LeufsTer?
ENST00000587648.5:c.375_379del ENSP00000468349.1:p.Phe125LeufsTer?
ENST00000588919.5:c.414_418del ENSP00000464989.3:p.Phe138LeufsTer19
ENST00000589115.5:c.477-140_477-136del ENSP00000466872.2:n.477-140_477-136del
ENST00000592940.2:n.866_870del
ENST00000593032.5:c.475_479del ENSP00000465828.3:p.His159SerfsTer11
ENST00000611653.4:c.414_418del ENSP00000483655.1:p.Phe138LeufsTer?
ENST00000616066.4:c.492_496del ENSP00000485000.1:p.Phe164LeufsTer?
ENST00000622390.4:c.603_607del ENSP00000477503.1:p.Phe201LeufsTer?
NM_001039847.2:c.495_499del NP_001034936.1:p.Phe165LeufsTer19
NM_001039848.2:c.606_610del NP_001034937.1:p.Phe202LeufsTer?
NM_002085.4:c.495_499del NP_002076.2:p.Phe165LeufsTer?
NM_001039848.3:c.606_610del NP_001034937.1:p.Phe202LeufsTer?
NM_001039847.3:c.495_499del NP_001034936.1:p.Phe165LeufsTer19
NM_001039848.4:c.606_610del NP_001034937.1:p.Phe202LeufsTer?
NM_001367832.1:c.414_418del NP_001354761.1:p.Phe138LeufsTer?
NM_002085.5:c.495_499del MANE Select NP_002076.2:p.Phe165LeufsTer?