Canonical Allele Identifier: CA402934150
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1104049-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104049C>G , CM000681.2:g.1104049C>G GRCh38
NC_000019.9:g.1104048C>G , CM000681.1:g.1104048C>G GRCh37
NC_000019.8:g.1055048C>G NCBI36
NG_050621.1:g.5124C>G

Transcript Alleles

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