Canonical Allele Identifier: CA402939162

Gene: GPX4

Linked Data

• gnomAD v3: 19-1106252-T-G
• gnomAD v4: 19-1106252-T-G
• MyVariant Identifiers: chr19:g.1106251T>G (hg19) ; chr19:g.1106252T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106252T>G , CM000681.2:g.1106252T>G	GRCh38
NC_000019.9:g.1106251T>G , CM000681.1:g.1106251T>G	GRCh37
NC_000019.8:g.1057251T>G	NCBI36
NG_050621.1:g.7327T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.598T>G	ENSP00000473614.3:p.Trp200Gly
ENST00000593032.6:c.467T>G	ENSP00000465828.4:p.Val156Gly
ENST00000706713.1:c.481T>G	ENSP00000516510.1:p.Trp161Gly
ENST00000706714.1:c.467T>G	ENSP00000516511.1:p.Val156Gly
ENST00000706715.1:c.103T>G	ENSP00000516512.1:p.Trp35Gly
ENST00000354171.13:c.487T>G MANE Select	ENSP00000346103.7:p.Trp163Gly
ENST00000589115.6:c.477-148T>G	ENSP00000466872.3:n.477-148T>G
ENST00000354171.12:c.487T>G	ENSP00000346103.7:p.Trp163Gly
ENST00000585480.1:c.220T>G	ENSP00000467900.1:p.Trp74Gly
ENST00000587648.5:c.367T>G	ENSP00000468349.1:p.Trp123Gly
ENST00000588919.5:c.406T>G	ENSP00000464989.3:p.Trp136Gly
ENST00000589115.5:c.477-148T>G	ENSP00000466872.2:n.477-148T>G
ENST00000592940.2:n.858T>G
ENST00000593032.5:c.467T>G	ENSP00000465828.3:p.Val156Gly
ENST00000611653.4:c.406T>G	ENSP00000483655.1:p.Trp136Gly
ENST00000616066.4:c.484T>G	ENSP00000485000.1:p.Trp162Gly
ENST00000622390.4:c.595T>G	ENSP00000477503.1:p.Trp199Gly
NM_001039847.2:c.487T>G	NP_001034936.1:p.Trp163Gly
NM_001039848.2:c.598T>G	NP_001034937.1:p.Trp200Gly
NM_002085.4:c.487T>G	NP_002076.2:p.Trp163Gly
NM_001039848.3:c.598T>G	NP_001034937.1:p.Trp200Gly
NM_001039847.3:c.487T>G	NP_001034936.1:p.Trp163Gly
NM_001039848.4:c.598T>G	NP_001034937.1:p.Trp200Gly
NM_001367832.1:c.406T>G	NP_001354761.1:p.Trp136Gly
NM_002085.5:c.487T>G MANE Select	NP_002076.2:p.Trp163Gly