Canonical Allele Identifier: CA402940121

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106449G>A (hg19) ; chr19:g.1106450G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106450G>A , CM000681.2:g.1106450G>A	GRCh38
NC_000019.9:g.1106449G>A , CM000681.1:g.1106449G>A	GRCh37
NC_000019.8:g.1057449G>A	NCBI36
NG_050621.1:g.7525G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.663G>A	ENSP00000473614.3:p.Glu221=
ENST00000593032.6:c.532G>A	ENSP00000465828.4:p.Gly178Arg
ENST00000706713.1:c.546G>A	ENSP00000516510.1:p.Glu182=
ENST00000706714.1:c.532G>A	ENSP00000516511.1:p.Gly178Arg
ENST00000706715.1:c.168G>A	ENSP00000516512.1:p.Glu56=
ENST00000354171.13:c.552G>A MANE Select	ENSP00000346103.7:p.Glu184=
ENST00000589115.6:c.527G>A	ENSP00000466872.3:p.Arg176Lys
ENST00000354171.12:c.552G>A	ENSP00000346103.7:p.Glu184=
ENST00000585480.1:c.285G>A	ENSP00000467900.1:p.Glu95=
ENST00000587648.5:c.432G>A	ENSP00000468349.1:p.Glu144=
ENST00000588919.5:c.493G>A	ENSP00000464989.3:p.Gly165Arg
ENST00000589115.5:c.527G>A	ENSP00000466872.2:p.Arg176Lys
ENST00000592940.2:n.923G>A
ENST00000611653.4:c.471G>A	ENSP00000483655.1:p.Glu157=
ENST00000616066.4:c.549G>A	ENSP00000485000.1:p.Glu183=
ENST00000622390.4:c.660G>A	ENSP00000477503.1:p.Glu220=
NM_001039847.2:c.574G>A	NP_001034936.1:p.Gly192Arg
NM_001039848.2:c.663G>A	NP_001034937.1:p.Glu221=
NM_002085.4:c.552G>A	NP_002076.2:p.Glu184=
NM_001039848.3:c.663G>A	NP_001034937.1:p.Glu221=
NM_001039847.3:c.574G>A	NP_001034936.1:p.Gly192Arg
NM_001039848.4:c.663G>A	NP_001034937.1:p.Glu221=
NM_001367832.1:c.471G>A	NP_001354761.1:p.Glu157=
NM_002085.5:c.552G>A MANE Select	NP_002076.2:p.Glu184=