Canonical Allele Identifier: CA2813238230
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104029C>A , CM000681.2:g.1104029C>A GRCh38
NC_000019.9:g.1104028C>A , CM000681.1:g.1104028C>A GRCh37
NC_000019.8:g.1055028C>A NCBI36
NG_050621.1:g.5104C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706713.1:c.-15C>A ENSP00000516510.1:n.-15C>A
ENST00000354171.13:c.-15C>A MANE Select ENSP00000346103.7:n.-15C>A
ENST00000589115.6:c.-15C>A ENSP00000466872.3:n.-15C>A
ENST00000354171.12:c.-15C>A ENSP00000346103.7:n.-15C>A
ENST00000589115.5:c.-15C>A ENSP00000466872.2:n.-15C>A
ENST00000616066.4:c.-15C>A ENSP00000485000.1:n.-15C>A
NM_001039847.2:c.-15C>A NP_001034936.1:n.-15C>A
NM_002085.4:c.-15C>A NP_002076.2:n.-15C>A
NM_001039847.3:c.-15C>A NP_001034936.1:n.-15C>A
NM_002085.5:c.-15C>A MANE Select NP_002076.2:n.-15C>A