Canonical Allele Identifier: CA2576545169
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106414_1106415del , CM000681.2:g.1106414_1106415del GRCh38
NC_000019.9:g.1106413_1106414del , CM000681.1:g.1106413_1106414del GRCh37
NC_000019.8:g.1057413_1057414del NCBI36
NG_050621.1:g.7489_7490del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.627_628del ENSP00000473614.3:p.Asn210ArgfsTer?
ENST00000593032.6:c.496_497del ENSP00000465828.4:p.Glu166ThrfsTer5
ENST00000706713.1:c.510_511del ENSP00000516510.1:p.Asn171ArgfsTer?
ENST00000706714.1:c.496_497del ENSP00000516511.1:p.Glu166ThrfsTer5
ENST00000706715.1:c.132_133del ENSP00000516512.1:p.Asn45ArgfsTer?
ENST00000354171.13:c.516_517del MANE Select ENSP00000346103.7:p.Asn173ArgfsTer?
ENST00000589115.6:c.491_492del ENSP00000466872.3:p.Arg164AsnfsTer26
ENST00000354171.12:c.516_517del ENSP00000346103.7:p.Asn173ArgfsTer?
ENST00000585480.1:c.249_250del ENSP00000467900.1:p.Asn84ArgfsTer?
ENST00000587648.5:c.396_397del ENSP00000468349.1:p.Asn133ArgfsTer?
ENST00000588919.5:c.457_458del ENSP00000464989.3:p.Glu153ThrfsTer5
ENST00000589115.5:c.491_492del ENSP00000466872.2:p.Arg164AsnfsTer26
ENST00000592940.2:n.887_888del
ENST00000593032.5:c.496_497del ENSP00000465828.3:p.Glu166ThrfsTer5
ENST00000611653.4:c.435_436del ENSP00000483655.1:p.Asn146ArgfsTer?
ENST00000616066.4:c.513_514del ENSP00000485000.1:p.Asn172ArgfsTer?
ENST00000622390.4:c.624_625del ENSP00000477503.1:p.Asn209ArgfsTer?
NM_001039847.2:c.538_539del NP_001034936.1:p.Glu180ThrfsTer5
NM_001039848.2:c.627_628del NP_001034937.1:p.Asn210ArgfsTer?
NM_002085.4:c.516_517del NP_002076.2:p.Asn173ArgfsTer?
NM_001039848.3:c.627_628del NP_001034937.1:p.Asn210ArgfsTer?
NM_001039847.3:c.538_539del NP_001034936.1:p.Glu180ThrfsTer5
NM_001039848.4:c.627_628del NP_001034937.1:p.Asn210ArgfsTer?
NM_001367832.1:c.435_436del NP_001354761.1:p.Asn146ArgfsTer?
NM_002085.5:c.516_517del MANE Select NP_002076.2:p.Asn173ArgfsTer?