Canonical Allele Identifier: CA2588207516
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106033_1106095del , CM000681.2:g.1106033_1106095del GRCh38
NC_000019.9:g.1106032_1106094del , CM000681.1:g.1106032_1106094del GRCh37
NC_000019.8:g.1057032_1057094del NCBI36
NG_050621.1:g.7108_7170del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.588-209_588-147del ENSP00000473614.3:n.588-209_588-147del
ENST00000593032.6:c.396-148_396-86del ENSP00000465828.4:n.396-148_396-86del
ENST00000706713.1:c.471-209_471-147del ENSP00000516510.1:n.471-209_471-147del
ENST00000706714.1:c.396-148_396-86del ENSP00000516511.1:n.396-148_396-86del
ENST00000706715.1:c.93-209_93-147del ENSP00000516512.1:n.93-209_93-147del
ENST00000354171.13:c.477-209_477-147del MANE Select ENSP00000346103.7:n.477-209_477-147del
ENST00000589115.6:c.476+224_476+286del ENSP00000466872.3:n.476+224_476+286del
ENST00000354171.12:c.477-209_477-147del ENSP00000346103.7:n.477-209_477-147del
ENST00000585480.1:c.210-209_210-147del ENSP00000467900.1:n.210-209_210-147del
ENST00000587648.5:c.357-209_357-147del ENSP00000468349.1:n.357-209_357-147del
ENST00000588919.5:c.396-209_396-147del ENSP00000464989.3:n.396-209_396-147del
ENST00000589115.5:c.476+224_476+286del ENSP00000466872.2:n.476+224_476+286del
ENST00000592940.2:n.639_701del
ENST00000593032.5:c.396-148_396-86del ENSP00000465828.3:n.396-148_396-86del
ENST00000611653.4:c.396-209_396-147del ENSP00000483655.1:n.396-209_396-147del
ENST00000616066.4:c.474-209_474-147del ENSP00000485000.1:n.474-209_474-147del
ENST00000622390.4:c.585-209_585-147del ENSP00000477503.1:n.585-209_585-147del
NM_001039847.2:c.477-209_477-147del NP_001034936.1:n.477-209_477-147del
NM_001039848.2:c.588-209_588-147del NP_001034937.1:n.588-209_588-147del
NM_002085.4:c.477-209_477-147del NP_002076.2:n.477-209_477-147del
NM_001039848.3:c.588-209_588-147del NP_001034937.1:n.588-209_588-147del
NM_001039847.3:c.477-209_477-147del NP_001034936.1:n.477-209_477-147del
NM_001039848.4:c.588-209_588-147del NP_001034937.1:n.588-209_588-147del
NM_001367832.1:c.396-209_396-147del NP_001354761.1:n.396-209_396-147del
NM_002085.5:c.477-209_477-147del MANE Select NP_002076.2:n.477-209_477-147del