Canonical Allele Identifier: CA2317520663

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106438C= , CM000681.2:g.1106438C=	GRCh38
NC_000019.9:g.1106437C= , CM000681.1:g.1106437C=	GRCh37
NC_000019.8:g.1057437C=	NCBI36
NG_050621.1:g.7513C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.651C=	ENSP00000473614.3:p.Tyr217=
ENST00000593032.6:c.520C=	ENSP00000465828.4:p.Arg174=
ENST00000706713.1:c.534C=	ENSP00000516510.1:p.Tyr178=
ENST00000706714.1:c.520C=	ENSP00000516511.1:p.Arg174=
ENST00000706715.1:c.156C=	ENSP00000516512.1:p.Tyr52=
ENST00000354171.13:c.540C= MANE Select	ENSP00000346103.7:p.Tyr180=
ENST00000589115.6:c.515C=	ENSP00000466872.3:p.Thr172=
ENST00000354171.12:c.540C=	ENSP00000346103.7:p.Tyr180=
ENST00000585480.1:c.273C=	ENSP00000467900.1:p.Tyr91=
ENST00000587648.5:c.420C=	ENSP00000468349.1:p.Tyr140=
ENST00000588919.5:c.481C=	ENSP00000464989.3:p.Arg161=
ENST00000589115.5:c.515C=	ENSP00000466872.2:p.Thr172=
ENST00000592940.2:n.911C=
ENST00000593032.5:c.520C=	ENSP00000465828.3:p.Arg174=
ENST00000611653.4:c.459C=	ENSP00000483655.1:p.Tyr153=
ENST00000616066.4:c.537C=	ENSP00000485000.1:p.Tyr179=
ENST00000622390.4:c.648C=	ENSP00000477503.1:p.Tyr216=
NM_001039847.2:c.562C=	NP_001034936.1:p.Arg188=
NM_001039848.2:c.651C=	NP_001034937.1:p.Tyr217=
NM_002085.4:c.540C=	NP_002076.2:p.Tyr180=
NM_001039848.3:c.651C=	NP_001034937.1:p.Tyr217=
NM_001039847.3:c.562C=	NP_001034936.1:p.Arg188=
NM_001039848.4:c.651C=	NP_001034937.1:p.Tyr217=
NM_001367832.1:c.459C=	NP_001354761.1:p.Tyr153=
NM_002085.5:c.540C= MANE Select	NP_002076.2:p.Tyr180=