Canonical Allele Identifier: CA402940163

Gene: GPX4

Linked Data

• dbSNP Id: rs1422303673
• gnomAD v2: 19-1106453-C-A
• gnomAD v4: 19-1106454-C-A
• MyVariant Identifiers: chr19:g.1106453C>A (hg19) ; chr19:g.1106454C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106454C>A , CM000681.2:g.1106454C>A	GRCh38
NC_000019.9:g.1106453C>A , CM000681.1:g.1106453C>A	GRCh37
NC_000019.8:g.1057453C>A	NCBI36
NG_050621.1:g.7529C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.667C>A	ENSP00000473614.3:p.Pro223Thr
ENST00000593032.6:c.536C>A	ENSP00000465828.4:p.Ala179Asp
ENST00000706713.1:c.550C>A	ENSP00000516510.1:p.Pro184Thr
ENST00000706714.1:c.536C>A	ENSP00000516511.1:p.Ala179Asp
ENST00000706715.1:c.172C>A	ENSP00000516512.1:p.Pro58Thr
ENST00000354171.13:c.556C>A MANE Select	ENSP00000346103.7:p.Pro186Thr
ENST00000589115.6:c.531C>A	ENSP00000466872.3:p.Ser177Arg
ENST00000354171.12:c.556C>A	ENSP00000346103.7:p.Pro186Thr
ENST00000585480.1:c.289C>A	ENSP00000467900.1:p.Pro97Thr
ENST00000587648.5:c.436C>A	ENSP00000468349.1:p.Pro146Thr
ENST00000588919.5:c.497C>A	ENSP00000464989.3:p.Ala166Asp
ENST00000589115.5:c.531C>A	ENSP00000466872.2:p.Ser177Arg
ENST00000592940.2:n.927C>A
ENST00000611653.4:c.475C>A	ENSP00000483655.1:p.Pro159Thr
ENST00000616066.4:c.553C>A	ENSP00000485000.1:p.Pro185Thr
ENST00000622390.4:c.664C>A	ENSP00000477503.1:p.Pro222Thr
NM_001039847.2:c.578C>A	NP_001034936.1:p.Ala193Asp
NM_001039848.2:c.667C>A	NP_001034937.1:p.Pro223Thr
NM_002085.4:c.556C>A	NP_002076.2:p.Pro186Thr
NM_001039848.3:c.667C>A	NP_001034937.1:p.Pro223Thr
NM_001039847.3:c.578C>A	NP_001034936.1:p.Ala193Asp
NM_001039848.4:c.667C>A	NP_001034937.1:p.Pro223Thr
NM_001367832.1:c.475C>A	NP_001354761.1:p.Pro159Thr
NM_002085.5:c.556C>A MANE Select	NP_002076.2:p.Pro186Thr