Canonical Allele Identifier: CA2317518953
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103965A= , CM000681.2:g.1103965A= GRCh38
NC_000019.9:g.1103964A= , CM000681.1:g.1103964A= GRCh37
NC_000019.8:g.1054964A= NCBI36
NG_050621.1:g.5040A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.-79A= ENSP00000346103.7:n.-79A=
ENST00000616066.4:c.-79A= ENSP00000485000.1:n.-79A=
NM_001039847.2:c.-79A= NP_001034936.1:n.-79A=
NM_002085.4:c.-79A= NP_002076.2:n.-79A=