Canonical Allele Identifier: CA2317520526

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106260C= , CM000681.2:g.1106260C=	GRCh38
NC_000019.9:g.1106259C= , CM000681.1:g.1106259C=	GRCh37
NC_000019.8:g.1057259C=	NCBI36
NG_050621.1:g.7335C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.606C=	ENSP00000473614.3:p.Phe202=
ENST00000593032.6:c.475C=	ENSP00000465828.4:p.His159=
ENST00000706713.1:c.489C=	ENSP00000516510.1:p.Phe163=
ENST00000706714.1:c.475C=	ENSP00000516511.1:p.His159=
ENST00000706715.1:c.111C=	ENSP00000516512.1:p.Phe37=
ENST00000354171.13:c.495C= MANE Select	ENSP00000346103.7:p.Phe165=
ENST00000589115.6:c.477-140C=	ENSP00000466872.3:n.477-140C=
ENST00000354171.12:c.495C=	ENSP00000346103.7:p.Phe165=
ENST00000585480.1:c.228C=	ENSP00000467900.1:p.Phe76=
ENST00000587648.5:c.375C=	ENSP00000468349.1:p.Phe125=
ENST00000588919.5:c.414C=	ENSP00000464989.3:p.Phe138=
ENST00000589115.5:c.477-140C=	ENSP00000466872.2:n.477-140C=
ENST00000592940.2:n.866C=
ENST00000593032.5:c.475C=	ENSP00000465828.3:p.His159=
ENST00000611653.4:c.414C=	ENSP00000483655.1:p.Phe138=
ENST00000616066.4:c.492C=	ENSP00000485000.1:p.Phe164=
ENST00000622390.4:c.603C=	ENSP00000477503.1:p.Phe201=
NM_001039847.2:c.495C=	NP_001034936.1:p.Phe165=
NM_001039848.2:c.606C=	NP_001034937.1:p.Phe202=
NM_002085.4:c.495C=	NP_002076.2:p.Phe165=
NM_001039848.3:c.606C=	NP_001034937.1:p.Phe202=
NM_001039847.3:c.495C=	NP_001034936.1:p.Phe165=
NM_001039848.4:c.606C=	NP_001034937.1:p.Phe202=
NM_001367832.1:c.414C=	NP_001354761.1:p.Phe138=
NM_002085.5:c.495C= MANE Select	NP_002076.2:p.Phe165=