Canonical Allele Identifier: CA2317519009
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104033G= , CM000681.2:g.1104033G= GRCh38
NC_000019.9:g.1104032G= , CM000681.1:g.1104032G= GRCh37
NC_000019.8:g.1055032G= NCBI36
NG_050621.1:g.5108G=

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-11G= ENSP00000516510.1:n.-11G=
ENST00000354171.13:c.-11G= MANE Select ENSP00000346103.7:n.-11G=
ENST00000589115.6:c.-11G= ENSP00000466872.3:n.-11G=
ENST00000354171.12:c.-11G= ENSP00000346103.7:n.-11G=
ENST00000589115.5:c.-11G= ENSP00000466872.2:n.-11G=
ENST00000616066.4:c.-11G= ENSP00000485000.1:n.-11G=
NM_001039847.2:c.-11G= NP_001034936.1:n.-11G=
NM_002085.4:c.-11G= NP_002076.2:n.-11G=
NM_001039847.3:c.-11G= NP_001034936.1:n.-11G=
NM_002085.5:c.-11G= MANE Select NP_002076.2:n.-11G=