Canonical Allele Identifier: CA2588207943

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106752-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106754del , CM000681.2:g.1106754del	GRCh38
NC_000019.9:g.1106753del , CM000681.1:g.1106753del	GRCh37
NC_000019.8:g.1057753del	NCBI36
NG_050621.1:g.7829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*182del	ENSP00000473614.3:n.*182del
ENST00000593032.6:c.756del	ENSP00000465828.4:p.Leu253CysfsTer?
ENST00000706713.1:c.*182del	ENSP00000516510.1:n.*182del
ENST00000706714.1:c.756del	ENSP00000516511.1:p.Leu253CysfsTer?
ENST00000706715.1:c.*182del	ENSP00000516512.1:n.*182del
ENST00000354171.13:c.*182del MANE Select	ENSP00000346103.7:n.*182del
ENST00000589115.6:c.*208del	ENSP00000466872.3:n.*208del
ENST00000354171.12:c.*182del	ENSP00000346103.7:n.*182del
ENST00000585480.1:c.476del	ENSP00000467900.1:p.Pro159LeufsTer?
ENST00000588919.5:c.717del	ENSP00000464989.3:p.Leu240CysfsTer8
ENST00000589115.5:c.*208del	ENSP00000466872.2:n.*208del
ENST00000592940.2:n.1147del
ENST00000611653.4:c.*182del	ENSP00000483655.1:n.*182del
ENST00000616066.4:c.*182del	ENSP00000485000.1:n.*182del
ENST00000622390.4:c.*182del	ENSP00000477503.1:n.*182del
NM_001039847.2:c.*114del	NP_001034936.1:n.*114del
NM_001039848.2:c.*182del	NP_001034937.1:n.*182del
NM_002085.4:c.*182del	NP_002076.2:n.*182del
NM_001039848.3:c.*182del	NP_001034937.1:n.*182del
NM_001039847.3:c.*114del	NP_001034936.1:n.*114del
NM_001039848.4:c.*182del	NP_001034937.1:n.*182del
NM_001367832.1:c.*182del	NP_001354761.1:n.*182del
NM_002085.5:c.*182del MANE Select	NP_002076.2:n.*182del