Canonical Allele Identifier: CA2527906136

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106122_1106123insTAGCTGCC , CM000681.2:g.1106122_1106123insTAGCTGCC	GRCh38
NC_000019.9:g.1106121_1106122insTAGCTGCC , CM000681.1:g.1106121_1106122insTAGCTGCC	GRCh37
NC_000019.8:g.1057121_1057122insTAGCTGCC	NCBI36
NG_050621.1:g.7197_7198insTAGCTGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-120_588-119insTAGCTGCC	ENSP00000473614.3:n.588-120_588-119insTAGCTGCC
ENST00000593032.6:c.396-59_396-58insTAGCTGCC	ENSP00000465828.4:n.396-59_396-58insTAGCTGCC
ENST00000706713.1:c.471-120_471-119insTAGCTGCC	ENSP00000516510.1:n.471-120_471-119insTAGCTGCC
ENST00000706714.1:c.396-59_396-58insTAGCTGCC	ENSP00000516511.1:n.396-59_396-58insTAGCTGCC
ENST00000706715.1:c.93-120_93-119insTAGCTGCC	ENSP00000516512.1:n.93-120_93-119insTAGCTGCC
ENST00000354171.13:c.477-120_477-119insTAGCTGCC MANE Select	ENSP00000346103.7:n.477-120_477-119insTAGCTGCC
ENST00000589115.6:c.477-278_477-277insTAGCTGCC	ENSP00000466872.3:n.477-278_477-277insTAGCTGCC
ENST00000354171.12:c.477-120_477-119insTAGCTGCC	ENSP00000346103.7:n.477-120_477-119insTAGCTGCC
ENST00000585480.1:c.210-120_210-119insTAGCTGCC	ENSP00000467900.1:n.210-120_210-119insTAGCTGCC
ENST00000587648.5:c.357-120_357-119insTAGCTGCC	ENSP00000468349.1:n.357-120_357-119insTAGCTGCC
ENST00000588919.5:c.396-120_396-119insTAGCTGCC	ENSP00000464989.3:n.396-120_396-119insTAGCTGCC
ENST00000589115.5:c.477-278_477-277insTAGCTGCC	ENSP00000466872.2:n.477-278_477-277insTAGCTGCC
ENST00000592940.2:n.728_729insTAGCTGCC
ENST00000593032.5:c.396-59_396-58insTAGCTGCC	ENSP00000465828.3:n.396-59_396-58insTAGCTGCC
ENST00000611653.4:c.396-120_396-119insTAGCTGCC	ENSP00000483655.1:n.396-120_396-119insTAGCTGCC
ENST00000616066.4:c.474-120_474-119insTAGCTGCC	ENSP00000485000.1:n.474-120_474-119insTAGCTGCC
ENST00000622390.4:c.585-120_585-119insTAGCTGCC	ENSP00000477503.1:n.585-120_585-119insTAGCTGCC
NM_001039847.2:c.477-120_477-119insTAGCTGCC	NP_001034936.1:n.477-120_477-119insTAGCTGCC
NM_001039848.2:c.588-120_588-119insTAGCTGCC	NP_001034937.1:n.588-120_588-119insTAGCTGCC
NM_002085.4:c.477-120_477-119insTAGCTGCC	NP_002076.2:n.477-120_477-119insTAGCTGCC
NM_001039848.3:c.588-120_588-119insTAGCTGCC	NP_001034937.1:n.588-120_588-119insTAGCTGCC
NM_001039847.3:c.477-120_477-119insTAGCTGCC	NP_001034936.1:n.477-120_477-119insTAGCTGCC
NM_001039848.4:c.588-120_588-119insTAGCTGCC	NP_001034937.1:n.588-120_588-119insTAGCTGCC
NM_001367832.1:c.396-120_396-119insTAGCTGCC	NP_001354761.1:n.396-120_396-119insTAGCTGCC
NM_002085.5:c.477-120_477-119insTAGCTGCC MANE Select	NP_002076.2:n.477-120_477-119insTAGCTGCC