Canonical Allele Identifier: CA2317520522

Gene: GPX4

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.600G=	ENSP00000473614.3:p.Trp200=
ENST00000593032.6:c.469G=	ENSP00000465828.4:p.Glu157=
ENST00000706713.1:c.483G=	ENSP00000516510.1:p.Trp161=
ENST00000706714.1:c.469G=	ENSP00000516511.1:p.Glu157=
ENST00000706715.1:c.105G=	ENSP00000516512.1:p.Trp35=
ENST00000354171.13:c.489G= MANE Select	ENSP00000346103.7:p.Trp163=
ENST00000589115.6:c.477-146G=	ENSP00000466872.3:n.477-146G=
ENST00000354171.12:c.489G=	ENSP00000346103.7:p.Trp163=
ENST00000585480.1:c.222G=	ENSP00000467900.1:p.Trp74=
ENST00000587648.5:c.369G=	ENSP00000468349.1:p.Trp123=
ENST00000588919.5:c.408G=	ENSP00000464989.3:p.Trp136=
ENST00000589115.5:c.477-146G=	ENSP00000466872.2:n.477-146G=
ENST00000592940.2:n.860G=
ENST00000593032.5:c.469G=	ENSP00000465828.3:p.Glu157=
ENST00000611653.4:c.408G=	ENSP00000483655.1:p.Trp136=
ENST00000616066.4:c.486G=	ENSP00000485000.1:p.Trp162=
ENST00000622390.4:c.597G=	ENSP00000477503.1:p.Trp199=
NM_001039847.2:c.489G=	NP_001034936.1:p.Trp163=
NM_001039848.2:c.600G=	NP_001034937.1:p.Trp200=
NM_002085.4:c.489G=	NP_002076.2:p.Trp163=
NM_001039848.3:c.600G=	NP_001034937.1:p.Trp200=
NM_001039847.3:c.489G=	NP_001034936.1:p.Trp163=
NM_001039848.4:c.600G=	NP_001034937.1:p.Trp200=
NM_001367832.1:c.408G=	NP_001354761.1:p.Trp136=
NM_002085.5:c.489G= MANE Select	NP_002076.2:p.Trp163=