Canonical Allele Identifier: CA2317518979
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1103985C= , CM000681.2:g.1103985C= GRCh38
NC_000019.9:g.1103984C= , CM000681.1:g.1103984C= GRCh37
NC_000019.8:g.1054984C= NCBI36
NG_050621.1:g.5060C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706713.1:c.-59C= ENSP00000516510.1:n.-59C=
ENST00000354171.12:c.-59C= ENSP00000346103.7:n.-59C=
ENST00000616066.4:c.-59C= ENSP00000485000.1:n.-59C=
NM_001039847.2:c.-59C= NP_001034936.1:n.-59C=
NM_002085.4:c.-59C= NP_002076.2:n.-59C=