Canonical Allele Identifier: CA2317520670

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106447G= , CM000681.2:g.1106447G=	GRCh38
NC_000019.9:g.1106446G= , CM000681.1:g.1106446G=	GRCh37
NC_000019.8:g.1057446G=	NCBI36
NG_050621.1:g.7522G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.660G=	ENSP00000473614.3:p.Met220=
ENST00000593032.6:c.529G=	ENSP00000465828.4:p.Gly177=
ENST00000706713.1:c.543G=	ENSP00000516510.1:p.Met181=
ENST00000706714.1:c.529G=	ENSP00000516511.1:p.Gly177=
ENST00000706715.1:c.165G=	ENSP00000516512.1:p.Met55=
ENST00000354171.13:c.549G= MANE Select	ENSP00000346103.7:p.Met183=
ENST00000589115.6:c.524G=	ENSP00000466872.3:p.Trp175=
ENST00000354171.12:c.549G=	ENSP00000346103.7:p.Met183=
ENST00000585480.1:c.282G=	ENSP00000467900.1:p.Met94=
ENST00000587648.5:c.429G=	ENSP00000468349.1:p.Met143=
ENST00000588919.5:c.490G=	ENSP00000464989.3:p.Gly164=
ENST00000589115.5:c.524G=	ENSP00000466872.2:p.Trp175=
ENST00000592940.2:n.920G=
ENST00000611653.4:c.468G=	ENSP00000483655.1:p.Met156=
ENST00000616066.4:c.546G=	ENSP00000485000.1:p.Met182=
ENST00000622390.4:c.657G=	ENSP00000477503.1:p.Met219=
NM_001039847.2:c.571G=	NP_001034936.1:p.Gly191=
NM_001039848.2:c.660G=	NP_001034937.1:p.Met220=
NM_002085.4:c.549G=	NP_002076.2:p.Met183=
NM_001039848.3:c.660G=	NP_001034937.1:p.Met220=
NM_001039847.3:c.571G=	NP_001034936.1:p.Gly191=
NM_001039848.4:c.660G=	NP_001034937.1:p.Met220=
NM_001367832.1:c.468G=	NP_001354761.1:p.Met156=
NM_002085.5:c.549G= MANE Select	NP_002076.2:p.Met183=