Canonical Allele Identifier: CA402934143
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104046G>C , CM000681.2:g.1104046G>C GRCh38
NC_000019.9:g.1104045G>C , CM000681.1:g.1104045G>C GRCh37
NC_000019.8:g.1055045G>C NCBI36
NG_050621.1:g.5121G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.3G>C ENSP00000516510.1:p.Met1Ile
ENST00000354171.13:c.3G>C MANE Select ENSP00000346103.7:p.Met1Ile
ENST00000589115.6:c.3G>C ENSP00000466872.3:p.Met1Ile
ENST00000354171.12:c.3G>C ENSP00000346103.7:p.Met1Ile
ENST00000589115.5:c.3G>C ENSP00000466872.2:p.Met1Ile
ENST00000616066.4:c.3G>C ENSP00000485000.1:p.Met1Ile
NM_001039847.2:c.3G>C NP_001034936.1:p.Met1Ile
NM_002085.4:c.3G>C NP_002076.2:p.Met1Ile
NM_001039847.3:c.3G>C NP_001034936.1:p.Met1Ile
NM_002085.5:c.3G>C MANE Select NP_002076.2:p.Met1Ile