Canonical Allele Identifier: CA2588207966
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1106785-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106785T>A , CM000681.2:g.1106785T>A GRCh38
NC_000019.9:g.1106784T>A , CM000681.1:g.1106784T>A GRCh37
NC_000019.8:g.1057784T>A NCBI36
NG_050621.1:g.7860T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.*213T>A ENSP00000346103.7:n.*213T>A
ENST00000588919.5:c.*19T>A ENSP00000464989.3:n.*19T>A
ENST00000592940.2:n.1178T>A
ENST00000616066.4:c.*213T>A ENSP00000485000.1:n.*213T>A
ENST00000622390.4:c.*213T>A ENSP00000477503.1:n.*213T>A
NM_001039847.2:c.*145T>A NP_001034936.1:n.*145T>A
NM_001039848.2:c.*213T>A NP_001034937.1:n.*213T>A
NM_002085.4:c.*213T>A NP_002076.2:n.*213T>A
NM_001039848.3:c.*213T>A NP_001034937.1:n.*213T>A
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