Canonical Allele Identifier: CA402939175

Gene: GPX4

Linked Data

• dbSNP Id: rs893163820
• gnomAD v4: 19-1106254-G-A
• MyVariant Identifiers: chr19:g.1106253G>A (hg19) ; chr19:g.1106254G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106254G>A , CM000681.2:g.1106254G>A	GRCh38
NC_000019.9:g.1106253G>A , CM000681.1:g.1106253G>A	GRCh37
NC_000019.8:g.1057253G>A	NCBI36
NG_050621.1:g.7329G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.600G>A	ENSP00000473614.3:p.Trp200Ter
ENST00000593032.6:c.469G>A	ENSP00000465828.4:p.Glu157Lys
ENST00000706713.1:c.483G>A	ENSP00000516510.1:p.Trp161Ter
ENST00000706714.1:c.469G>A	ENSP00000516511.1:p.Glu157Lys
ENST00000706715.1:c.105G>A	ENSP00000516512.1:p.Trp35Ter
ENST00000354171.13:c.489G>A MANE Select	ENSP00000346103.7:p.Trp163Ter
ENST00000589115.6:c.477-146G>A	ENSP00000466872.3:n.477-146G>A
ENST00000354171.12:c.489G>A	ENSP00000346103.7:p.Trp163Ter
ENST00000585480.1:c.222G>A	ENSP00000467900.1:p.Trp74Ter
ENST00000587648.5:c.369G>A	ENSP00000468349.1:p.Trp123Ter
ENST00000588919.5:c.408G>A	ENSP00000464989.3:p.Trp136Ter
ENST00000589115.5:c.477-146G>A	ENSP00000466872.2:n.477-146G>A
ENST00000592940.2:n.860G>A
ENST00000593032.5:c.469G>A	ENSP00000465828.3:p.Glu157Lys
ENST00000611653.4:c.408G>A	ENSP00000483655.1:p.Trp136Ter
ENST00000616066.4:c.486G>A	ENSP00000485000.1:p.Trp162Ter
ENST00000622390.4:c.597G>A	ENSP00000477503.1:p.Trp199Ter
NM_001039847.2:c.489G>A	NP_001034936.1:p.Trp163Ter
NM_001039848.2:c.600G>A	NP_001034937.1:p.Trp200Ter
NM_002085.4:c.489G>A	NP_002076.2:p.Trp163Ter
NM_001039848.3:c.600G>A	NP_001034937.1:p.Trp200Ter
NM_001039847.3:c.489G>A	NP_001034936.1:p.Trp163Ter
NM_001039848.4:c.600G>A	NP_001034937.1:p.Trp200Ter
NM_001367832.1:c.408G>A	NP_001354761.1:p.Trp136Ter
NM_002085.5:c.489G>A MANE Select	NP_002076.2:p.Trp163Ter