Canonical Allele Identifier: CA2317520892
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106787G= , CM000681.2:g.1106787G= GRCh38
NC_000019.9:g.1106786G= , CM000681.1:g.1106786G= GRCh37
NC_000019.8:g.1057786G= NCBI36
NG_050621.1:g.7862G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.*215G= ENSP00000346103.7:n.*215G=
ENST00000588919.5:c.*21G= ENSP00000464989.3:n.*21G=
ENST00000592940.2:n.1180G=
ENST00000616066.4:c.*215G= ENSP00000485000.1:n.*215G=
ENST00000622390.4:c.*215G= ENSP00000477503.1:n.*215G=
NM_001039847.2:c.*147G= NP_001034936.1:n.*147G=
NM_001039848.2:c.*215G= NP_001034937.1:n.*215G=
NM_002085.4:c.*215G= NP_002076.2:n.*215G=
NM_001039848.3:c.*215G= NP_001034937.1:n.*215G=