Canonical Allele Identifier: CA402940423

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106567-T-G
• MyVariant Identifiers: chr19:g.1106566T>G (hg19) ; chr19:g.1106567T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106567T>G , CM000681.2:g.1106567T>G	GRCh38
NC_000019.9:g.1106566T>G , CM000681.1:g.1106566T>G	GRCh37
NC_000019.8:g.1057566T>G	NCBI36
NG_050621.1:g.7642T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.700T>G	ENSP00000473614.3:p.Phe234Val
ENST00000593032.6:c.569T>G	ENSP00000465828.4:p.Phe190Cys
ENST00000706713.1:c.583T>G	ENSP00000516510.1:p.Phe195Val
ENST00000706714.1:c.569T>G	ENSP00000516511.1:p.Phe190Cys
ENST00000706715.1:c.205T>G	ENSP00000516512.1:p.Phe69Val
ENST00000354171.13:c.589T>G MANE Select	ENSP00000346103.7:p.Phe197Val
ENST00000589115.6:c.*21T>G	ENSP00000466872.3:n.*21T>G
ENST00000354171.12:c.589T>G	ENSP00000346103.7:p.Phe197Val
ENST00000585480.1:c.295-6T>G	ENSP00000467900.1:n.295-6T>G
ENST00000588919.5:c.530T>G	ENSP00000464989.3:p.Phe177Cys
ENST00000589115.5:c.*21T>G	ENSP00000466872.2:n.*21T>G
ENST00000592940.2:n.960T>G
ENST00000611653.4:c.508T>G	ENSP00000483655.1:p.Phe170Val
ENST00000616066.4:c.586T>G	ENSP00000485000.1:p.Phe196Val
ENST00000622390.4:c.697T>G	ENSP00000477503.1:p.Phe233Val
NM_001039847.2:c.611T>G	NP_001034936.1:p.Phe204Cys
NM_001039848.2:c.700T>G	NP_001034937.1:p.Phe234Val
NM_002085.4:c.589T>G	NP_002076.2:p.Phe197Val
NM_001039848.3:c.700T>G	NP_001034937.1:p.Phe234Val
NM_001039847.3:c.611T>G	NP_001034936.1:p.Phe204Cys
NM_001039848.4:c.700T>G	NP_001034937.1:p.Phe234Val
NM_001367832.1:c.508T>G	NP_001354761.1:p.Phe170Val
NM_002085.5:c.589T>G MANE Select	NP_002076.2:p.Phe197Val