Canonical Allele Identifier: CA2576544971
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104010A>C , CM000681.2:g.1104010A>C GRCh38
NC_000019.9:g.1104009A>C , CM000681.1:g.1104009A>C GRCh37
NC_000019.8:g.1055009A>C NCBI36
NG_050621.1:g.5085A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-34A>C ENSP00000516510.1:n.-34A>C
ENST00000354171.13:c.-34A>C MANE Select ENSP00000346103.7:n.-34A>C
ENST00000589115.6:c.-34A>C ENSP00000466872.3:n.-34A>C
ENST00000354171.12:c.-34A>C ENSP00000346103.7:n.-34A>C
ENST00000589115.5:c.-34A>C ENSP00000466872.2:n.-34A>C
ENST00000616066.4:c.-34A>C ENSP00000485000.1:n.-34A>C
NM_001039847.2:c.-34A>C NP_001034936.1:n.-34A>C
NM_002085.4:c.-34A>C NP_002076.2:n.-34A>C
NM_001039847.3:c.-34A>C NP_001034936.1:n.-34A>C
NM_002085.5:c.-34A>C MANE Select NP_002076.2:n.-34A>C