Canonical Allele Identifier: CA303992502
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs573390223
gnomAD v2: 19-1104049-C-A
gnomAD v3: 19-1104050-C-A
gnomAD v4: 19-1104050-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104050C>A , CM000681.2:g.1104050C>A GRCh38
NC_000019.9:g.1104049C>A , CM000681.1:g.1104049C>A GRCh37
NC_000019.8:g.1055049C>A NCBI36
NG_050621.1:g.5125C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.7C>A ENSP00000516510.1:p.Leu3Ile
ENST00000354171.13:c.7C>A MANE Select ENSP00000346103.7:p.Leu3Ile
ENST00000589115.6:c.7C>A ENSP00000466872.3:p.Leu3Ile
ENST00000354171.12:c.7C>A ENSP00000346103.7:p.Leu3Ile
ENST00000589115.5:c.7C>A ENSP00000466872.2:p.Leu3Ile
ENST00000616066.4:c.7C>A ENSP00000485000.1:p.Leu3Ile
NM_001039847.2:c.7C>A NP_001034936.1:p.Leu3Ile
NM_002085.4:c.7C>A NP_002076.2:p.Leu3Ile
NM_001039847.3:c.7C>A NP_001034936.1:p.Leu3Ile
NM_002085.5:c.7C>A MANE Select NP_002076.2:p.Leu3Ile