Canonical Allele Identifier: CA2588207785
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106204_1106207del , CM000681.2:g.1106204_1106207del GRCh38
NC_000019.9:g.1106203_1106206del , CM000681.1:g.1106203_1106206del GRCh37
NC_000019.8:g.1057203_1057206del NCBI36
NG_050621.1:g.7279_7282del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.588-38_588-35del ENSP00000473614.3:n.588-38_588-35del
ENST00000593032.6:c.419_422del ENSP00000465828.4:p.Ala140ValfsTer?
ENST00000706713.1:c.471-38_471-35del ENSP00000516510.1:n.471-38_471-35del
ENST00000706714.1:c.419_422del ENSP00000516511.1:p.Ala140ValfsTer?
ENST00000706715.1:c.93-38_93-35del ENSP00000516512.1:n.93-38_93-35del
ENST00000354171.13:c.477-38_477-35del MANE Select ENSP00000346103.7:n.477-38_477-35del
ENST00000589115.6:c.477-196_477-193del ENSP00000466872.3:n.477-196_477-193del
ENST00000354171.12:c.477-38_477-35del ENSP00000346103.7:n.477-38_477-35del
ENST00000585480.1:c.210-38_210-35del ENSP00000467900.1:n.210-38_210-35del
ENST00000587648.5:c.357-38_357-35del ENSP00000468349.1:n.357-38_357-35del
ENST00000588919.5:c.396-38_396-35del ENSP00000464989.3:n.396-38_396-35del
ENST00000589115.5:c.477-196_477-193del ENSP00000466872.2:n.477-196_477-193del
ENST00000592940.2:n.810_813del
ENST00000593032.5:c.419_422del ENSP00000465828.3:p.Ala140ValfsTer?
ENST00000611653.4:c.396-38_396-35del ENSP00000483655.1:n.396-38_396-35del
ENST00000616066.4:c.474-38_474-35del ENSP00000485000.1:n.474-38_474-35del
ENST00000622390.4:c.585-38_585-35del ENSP00000477503.1:n.585-38_585-35del
NM_001039847.2:c.477-38_477-35del NP_001034936.1:n.477-38_477-35del
NM_001039848.2:c.588-38_588-35del NP_001034937.1:n.588-38_588-35del
NM_002085.4:c.477-38_477-35del NP_002076.2:n.477-38_477-35del
NM_001039848.3:c.588-38_588-35del NP_001034937.1:n.588-38_588-35del
NM_001039847.3:c.477-38_477-35del NP_001034936.1:n.477-38_477-35del
NM_001039848.4:c.588-38_588-35del NP_001034937.1:n.588-38_588-35del
NM_001367832.1:c.396-38_396-35del NP_001354761.1:n.396-38_396-35del
NM_002085.5:c.477-38_477-35del MANE Select NP_002076.2:n.477-38_477-35del