Canonical Allele Identifier: CA2840851276

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106663del , CM000681.2:g.1106663del	GRCh38
NC_000019.9:g.1106662del , CM000681.1:g.1106662del	GRCh37
NC_000019.8:g.1057662del	NCBI36
NG_050621.1:g.7738del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*91del	ENSP00000473614.3:n.*91del
ENST00000593032.6:c.665del	ENSP00000465828.4:p.Gly222ValfsTer?
ENST00000706713.1:c.*91del	ENSP00000516510.1:n.*91del
ENST00000706714.1:c.665del	ENSP00000516511.1:p.Gly222ValfsTer?
ENST00000706715.1:c.*91del	ENSP00000516512.1:n.*91del
ENST00000354171.13:c.*91del MANE Select	ENSP00000346103.7:n.*91del
ENST00000589115.6:c.*117del	ENSP00000466872.3:n.*117del
ENST00000354171.12:c.*91del	ENSP00000346103.7:n.*91del
ENST00000585480.1:c.385del	ENSP00000467900.1:p.Val129TrpfsTer?
ENST00000588919.5:c.626del	ENSP00000464989.3:p.Gly209ValfsTer?
ENST00000589115.5:c.*117del	ENSP00000466872.2:n.*117del
ENST00000592940.2:n.1056del
ENST00000611653.4:c.*91del	ENSP00000483655.1:n.*91del
ENST00000616066.4:c.*91del	ENSP00000485000.1:n.*91del
ENST00000622390.4:c.*91del	ENSP00000477503.1:n.*91del
NM_001039847.2:c.*23del	NP_001034936.1:n.*23del
NM_001039848.2:c.*91del	NP_001034937.1:n.*91del
NM_002085.4:c.*91del	NP_002076.2:n.*91del
NM_001039848.3:c.*91del	NP_001034937.1:n.*91del
NM_001039847.3:c.*23del	NP_001034936.1:n.*23del
NM_001039848.4:c.*91del	NP_001034937.1:n.*91del
NM_001367832.1:c.*91del	NP_001354761.1:n.*91del
NM_002085.5:c.*91del MANE Select	NP_002076.2:n.*91del