Canonical Allele Identifier: CA2317520673

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106453G= , CM000681.2:g.1106453G=	GRCh38
NC_000019.9:g.1106452G= , CM000681.1:g.1106452G=	GRCh37
NC_000019.8:g.1057452G=	NCBI36
NG_050621.1:g.7528G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.666G=	ENSP00000473614.3:p.Glu222=
ENST00000593032.6:c.535G=	ENSP00000465828.4:p.Ala179=
ENST00000706713.1:c.549G=	ENSP00000516510.1:p.Glu183=
ENST00000706714.1:c.535G=	ENSP00000516511.1:p.Ala179=
ENST00000706715.1:c.171G=	ENSP00000516512.1:p.Glu57=
ENST00000354171.13:c.555G= MANE Select	ENSP00000346103.7:p.Glu185=
ENST00000589115.6:c.530G=	ENSP00000466872.3:p.Ser177=
ENST00000354171.12:c.555G=	ENSP00000346103.7:p.Glu185=
ENST00000585480.1:c.288G=	ENSP00000467900.1:p.Glu96=
ENST00000587648.5:c.435G=	ENSP00000468349.1:p.Glu145=
ENST00000588919.5:c.496G=	ENSP00000464989.3:p.Ala166=
ENST00000589115.5:c.530G=	ENSP00000466872.2:p.Ser177=
ENST00000592940.2:n.926G=
ENST00000611653.4:c.474G=	ENSP00000483655.1:p.Glu158=
ENST00000616066.4:c.552G=	ENSP00000485000.1:p.Glu184=
ENST00000622390.4:c.663G=	ENSP00000477503.1:p.Glu221=
NM_001039847.2:c.577G=	NP_001034936.1:p.Ala193=
NM_001039848.2:c.666G=	NP_001034937.1:p.Glu222=
NM_002085.4:c.555G=	NP_002076.2:p.Glu185=
NM_001039848.3:c.666G=	NP_001034937.1:p.Glu222=
NM_001039847.3:c.577G=	NP_001034936.1:p.Ala193=
NM_001039848.4:c.666G=	NP_001034937.1:p.Glu222=
NM_001367832.1:c.474G=	NP_001354761.1:p.Glu158=
NM_002085.5:c.555G= MANE Select	NP_002076.2:p.Glu185=