Canonical Allele Identifier: CA2588207774
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106157_1106220del , CM000681.2:g.1106157_1106220del GRCh38
NC_000019.9:g.1106156_1106219del , CM000681.1:g.1106156_1106219del GRCh37
NC_000019.8:g.1057156_1057219del NCBI36
NG_050621.1:g.7232_7295del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.588-85_588-22del ENSP00000473614.3:n.588-85_588-22del
ENST00000593032.6:c.396-24_435del
ENST00000706713.1:c.471-85_471-22del ENSP00000516510.1:n.471-85_471-22del
ENST00000706714.1:c.396-24_435del
ENST00000706715.1:c.93-85_93-22del ENSP00000516512.1:n.93-85_93-22del
ENST00000354171.13:c.477-85_477-22del MANE Select ENSP00000346103.7:n.477-85_477-22del
ENST00000589115.6:c.477-243_477-180del ENSP00000466872.3:n.477-243_477-180del
ENST00000354171.12:c.477-85_477-22del ENSP00000346103.7:n.477-85_477-22del
ENST00000585480.1:c.210-85_210-22del ENSP00000467900.1:n.210-85_210-22del
ENST00000587648.5:c.357-85_357-22del ENSP00000468349.1:n.357-85_357-22del
ENST00000588919.5:c.396-85_396-22del ENSP00000464989.3:n.396-85_396-22del
ENST00000589115.5:c.477-243_477-180del ENSP00000466872.2:n.477-243_477-180del
ENST00000592940.2:n.763_826del
ENST00000593032.5:c.396-24_435del
ENST00000611653.4:c.396-85_396-22del ENSP00000483655.1:n.396-85_396-22del
ENST00000616066.4:c.474-85_474-22del ENSP00000485000.1:n.474-85_474-22del
ENST00000622390.4:c.585-85_585-22del ENSP00000477503.1:n.585-85_585-22del
NM_001039847.2:c.477-85_477-22del NP_001034936.1:n.477-85_477-22del
NM_001039848.2:c.588-85_588-22del NP_001034937.1:n.588-85_588-22del
NM_002085.4:c.477-85_477-22del NP_002076.2:n.477-85_477-22del
NM_001039848.3:c.588-85_588-22del NP_001034937.1:n.588-85_588-22del
NM_001039847.3:c.477-85_477-22del NP_001034936.1:n.477-85_477-22del
NM_001039848.4:c.588-85_588-22del NP_001034937.1:n.588-85_588-22del
NM_001367832.1:c.396-85_396-22del NP_001354761.1:n.396-85_396-22del
NM_002085.5:c.477-85_477-22del MANE Select NP_002076.2:n.477-85_477-22del