Canonical Allele Identifier: CA2317520664

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106439G= , CM000681.2:g.1106439G=	GRCh38
NC_000019.9:g.1106438G= , CM000681.1:g.1106438G=	GRCh37
NC_000019.8:g.1057438G=	NCBI36
NG_050621.1:g.7514G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.652G=	ENSP00000473614.3:p.Gly218=
ENST00000593032.6:c.521G=	ENSP00000465828.4:p.Arg174=
ENST00000706713.1:c.535G=	ENSP00000516510.1:p.Gly179=
ENST00000706714.1:c.521G=	ENSP00000516511.1:p.Arg174=
ENST00000706715.1:c.157G=	ENSP00000516512.1:p.Gly53=
ENST00000354171.13:c.541G= MANE Select	ENSP00000346103.7:p.Gly181=
ENST00000589115.6:c.516G=	ENSP00000466872.3:p.Thr172=
ENST00000354171.12:c.541G=	ENSP00000346103.7:p.Gly181=
ENST00000585480.1:c.274G=	ENSP00000467900.1:p.Gly92=
ENST00000587648.5:c.421G=	ENSP00000468349.1:p.Gly141=
ENST00000588919.5:c.482G=	ENSP00000464989.3:p.Arg161=
ENST00000589115.5:c.516G=	ENSP00000466872.2:p.Thr172=
ENST00000592940.2:n.912G=
ENST00000593032.5:c.521G=	ENSP00000465828.3:p.Arg174=
ENST00000611653.4:c.460G=	ENSP00000483655.1:p.Gly154=
ENST00000616066.4:c.538G=	ENSP00000485000.1:p.Gly180=
ENST00000622390.4:c.649G=	ENSP00000477503.1:p.Gly217=
NM_001039847.2:c.563G=	NP_001034936.1:p.Arg188=
NM_001039848.2:c.652G=	NP_001034937.1:p.Gly218=
NM_002085.4:c.541G=	NP_002076.2:p.Gly181=
NM_001039848.3:c.652G=	NP_001034937.1:p.Gly218=
NM_001039847.3:c.563G=	NP_001034936.1:p.Arg188=
NM_001039848.4:c.652G=	NP_001034937.1:p.Gly218=
NM_001367832.1:c.460G=	NP_001354761.1:p.Gly154=
NM_002085.5:c.541G= MANE Select	NP_002076.2:p.Gly181=