Canonical Allele Identifier: CA2576545099

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105687del , CM000681.2:g.1105687del	GRCh38
NC_000019.9:g.1105686del , CM000681.1:g.1105686del	GRCh37
NC_000019.8:g.1056686del	NCBI36
NG_050621.1:g.6762del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.465del	ENSP00000473614.3:p.Glu155AspfsTer18
ENST00000593032.6:c.273del	ENSP00000465828.4:p.Glu91AspfsTer18
ENST00000706713.1:c.348del	ENSP00000516510.1:p.Glu116AspfsTer18
ENST00000706714.1:c.273del	ENSP00000516511.1:p.Glu91AspfsTer18
ENST00000706715.1:c.-31del	ENSP00000516512.1:n.-31del
ENST00000354171.13:c.354del MANE Select	ENSP00000346103.7:p.Glu118AspfsTer18
ENST00000589115.6:c.354del	ENSP00000466872.3:p.Glu118AspfsTer18
ENST00000354171.12:c.354del	ENSP00000346103.7:p.Glu118AspfsTer18
ENST00000585362.6:c.465del	ENSP00000473614.2:p.Glu155AspfsTer18
ENST00000585480.1:c.87del	ENSP00000467900.1:p.Glu29AspfsTer18
ENST00000587648.5:c.234del	ENSP00000468349.1:p.Glu78AspfsTer18
ENST00000588919.5:c.273del	ENSP00000464989.3:p.Glu91AspfsTer18
ENST00000589115.5:c.354del	ENSP00000466872.2:p.Glu118AspfsTer18
ENST00000592940.2:n.293del
ENST00000593032.5:c.273del	ENSP00000465828.3:p.Glu91AspfsTer18
ENST00000611653.4:c.273del	ENSP00000483655.1:p.Glu91AspfsTer18
ENST00000616066.4:c.351del	ENSP00000485000.1:p.Glu117AspfsTer18
ENST00000622390.4:c.462del	ENSP00000477503.1:p.Glu154AspfsTer18
NM_001039847.2:c.354del	NP_001034936.1:p.Glu118AspfsTer18
NM_001039848.2:c.465del	NP_001034937.1:p.Glu155AspfsTer18
NM_002085.4:c.354del	NP_002076.2:p.Glu118AspfsTer18
NM_001039848.3:c.465del	NP_001034937.1:p.Glu155AspfsTer18
NM_001039847.3:c.354del	NP_001034936.1:p.Glu118AspfsTer18
NM_001039848.4:c.465del	NP_001034937.1:p.Glu155AspfsTer18
NM_001367832.1:c.273del	NP_001354761.1:p.Glu91AspfsTer18
NM_002085.5:c.354del MANE Select	NP_002076.2:p.Glu118AspfsTer18