Canonical Allele Identifier: CA2317518974
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103982C= , CM000681.2:g.1103982C= GRCh38
NC_000019.9:g.1103981C= , CM000681.1:g.1103981C= GRCh37
NC_000019.8:g.1054981C= NCBI36
NG_050621.1:g.5057C=

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-62C= ENSP00000516510.1:n.-62C=
ENST00000354171.12:c.-62C= ENSP00000346103.7:n.-62C=
ENST00000616066.4:c.-62C= ENSP00000485000.1:n.-62C=
NM_001039847.2:c.-62C= NP_001034936.1:n.-62C=
NM_002085.4:c.-62C= NP_002076.2:n.-62C=