Canonical Allele Identifier: CA402934144
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104047A>C , CM000681.2:g.1104047A>C GRCh38
NC_000019.9:g.1104046A>C , CM000681.1:g.1104046A>C GRCh37
NC_000019.8:g.1055046A>C NCBI36
NG_050621.1:g.5122A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.4A>C ENSP00000516510.1:p.Ser2Arg
ENST00000354171.13:c.4A>C MANE Select ENSP00000346103.7:p.Ser2Arg
ENST00000589115.6:c.4A>C ENSP00000466872.3:p.Ser2Arg
ENST00000354171.12:c.4A>C ENSP00000346103.7:p.Ser2Arg
ENST00000589115.5:c.4A>C ENSP00000466872.2:p.Ser2Arg
ENST00000616066.4:c.4A>C ENSP00000485000.1:p.Ser2Arg
NM_001039847.2:c.4A>C NP_001034936.1:p.Ser2Arg
NM_002085.4:c.4A>C NP_002076.2:p.Ser2Arg
NM_001039847.3:c.4A>C NP_001034936.1:p.Ser2Arg
NM_002085.5:c.4A>C MANE Select NP_002076.2:p.Ser2Arg