Canonical Allele Identifier: CA2576545180

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106567_1106568del , CM000681.2:g.1106567_1106568del	GRCh38
NC_000019.9:g.1106566_1106567del , CM000681.1:g.1106566_1106567del	GRCh37
NC_000019.8:g.1057566_1057567del	NCBI36
NG_050621.1:g.7642_7643del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.700_701del	ENSP00000473614.3:p.Phe234LeufsTer24
ENST00000593032.6:c.569_570del	ENSP00000465828.4:p.Phe190SerfsTer?
ENST00000706713.1:c.583_584del	ENSP00000516510.1:p.Phe195LeufsTer24
ENST00000706714.1:c.569_570del	ENSP00000516511.1:p.Phe190SerfsTer?
ENST00000706715.1:c.205_206del	ENSP00000516512.1:p.Phe69LeufsTer24
ENST00000354171.13:c.589_590del MANE Select	ENSP00000346103.7:p.Phe197LeufsTer24
ENST00000589115.6:c.*21_*22del	ENSP00000466872.3:n.*21_*22del
ENST00000354171.12:c.589_590del	ENSP00000346103.7:p.Phe197LeufsTer24
ENST00000585480.1:c.295-6_295-5del	ENSP00000467900.1:n.295-6_295-5del
ENST00000588919.5:c.530_531del	ENSP00000464989.3:p.Phe177SerfsTer?
ENST00000589115.5:c.*21_*22del	ENSP00000466872.2:n.*21_*22del
ENST00000592940.2:n.960_961del
ENST00000611653.4:c.508_509del	ENSP00000483655.1:p.Phe170LeufsTer24
ENST00000616066.4:c.586_587del	ENSP00000485000.1:p.Phe196LeufsTer24
ENST00000622390.4:c.697_698del	ENSP00000477503.1:p.Phe233LeufsTer24
NM_001039847.2:c.611_612del	NP_001034936.1:p.Phe204SerfsTer?
NM_001039848.2:c.700_701del	NP_001034937.1:p.Phe234LeufsTer24
NM_002085.4:c.589_590del	NP_002076.2:p.Phe197LeufsTer24
NM_001039848.3:c.700_701del	NP_001034937.1:p.Phe234LeufsTer24
NM_001039847.3:c.611_612del	NP_001034936.1:p.Phe204SerfsTer?
NM_001039848.4:c.700_701del	NP_001034937.1:p.Phe234LeufsTer24
NM_001367832.1:c.508_509del	NP_001354761.1:p.Phe170LeufsTer24
NM_002085.5:c.589_590del MANE Select	NP_002076.2:p.Phe197LeufsTer24