Canonical Allele Identifier: CA2317520795
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106628C= , CM000681.2:g.1106628C= GRCh38
NC_000019.9:g.1106627C= , CM000681.1:g.1106627C= GRCh37
NC_000019.8:g.1057627C= NCBI36
NG_050621.1:g.7703C=

Transcript Alleles

HGVS Amino-acid change
ENST00000585362.7:c.*56C= ENSP00000473614.3:n.*56C=
ENST00000593032.6:c.630C= ENSP00000465828.4:p.His210=
ENST00000706713.1:c.*56C= ENSP00000516510.1:n.*56C=
ENST00000706714.1:c.630C= ENSP00000516511.1:p.His210=
ENST00000706715.1:c.*56C= ENSP00000516512.1:n.*56C=
ENST00000354171.13:c.*56C= MANE Select ENSP00000346103.7:n.*56C=
ENST00000589115.6:c.*82C= ENSP00000466872.3:n.*82C=
ENST00000354171.12:c.*56C= ENSP00000346103.7:n.*56C=
ENST00000585480.1:c.350C= ENSP00000467900.1:p.Thr117=
ENST00000588919.5:c.591C= ENSP00000464989.3:p.His197=
ENST00000589115.5:c.*82C= ENSP00000466872.2:n.*82C=
ENST00000592940.2:n.1021C=
ENST00000611653.4:c.*56C= ENSP00000483655.1:n.*56C=
ENST00000616066.4:c.*56C= ENSP00000485000.1:n.*56C=
ENST00000622390.4:c.*56C= ENSP00000477503.1:n.*56C=
NM_001039847.2:c.672C= NP_001034936.1:p.His224=
NM_001039848.2:c.*56C= NP_001034937.1:n.*56C=
NM_002085.4:c.*56C= NP_002076.2:n.*56C=
NM_001039848.3:c.*56C= NP_001034937.1:n.*56C=
NM_001039847.3:c.672C= NP_001034936.1:p.His224=
NM_001039848.4:c.*56C= NP_001034937.1:n.*56C=
NM_001367832.1:c.*56C= NP_001354761.1:n.*56C=
NM_002085.5:c.*56C= MANE Select NP_002076.2:n.*56C=