Canonical Allele Identifier: CA2813244031
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106789T>A , CM000681.2:g.1106789T>A GRCh38
NC_000019.9:g.1106788T>A , CM000681.1:g.1106788T>A GRCh37
NC_000019.8:g.1057788T>A NCBI36
NG_050621.1:g.7864T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.*217T>A ENSP00000346103.7:n.*217T>A
ENST00000592940.2:n.1182T>A
NM_001039847.2:c.*149T>A NP_001034936.1:n.*149T>A
NM_001039848.2:c.*217T>A NP_001034937.1:n.*217T>A
NM_002085.4:c.*217T>A NP_002076.2:n.*217T>A
NM_001039848.3:c.*217T>A NP_001034937.1:n.*217T>A