Canonical Allele Identifier: CA2317520668

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106445A= , CM000681.2:g.1106445A=	GRCh38
NC_000019.9:g.1106444A= , CM000681.1:g.1106444A=	GRCh37
NC_000019.8:g.1057444A=	NCBI36
NG_050621.1:g.7520A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.658A=	ENSP00000473614.3:p.Met220=
ENST00000593032.6:c.527A=	ENSP00000465828.4:p.His176=
ENST00000706713.1:c.541A=	ENSP00000516510.1:p.Met181=
ENST00000706714.1:c.527A=	ENSP00000516511.1:p.His176=
ENST00000706715.1:c.163A=	ENSP00000516512.1:p.Met55=
ENST00000354171.13:c.547A= MANE Select	ENSP00000346103.7:p.Met183=
ENST00000589115.6:c.522A=	ENSP00000466872.3:p.Pro174=
ENST00000354171.12:c.547A=	ENSP00000346103.7:p.Met183=
ENST00000585480.1:c.280A=	ENSP00000467900.1:p.Met94=
ENST00000587648.5:c.427A=	ENSP00000468349.1:p.Met143=
ENST00000588919.5:c.488A=	ENSP00000464989.3:p.His163=
ENST00000589115.5:c.522A=	ENSP00000466872.2:p.Pro174=
ENST00000592940.2:n.918A=
ENST00000611653.4:c.466A=	ENSP00000483655.1:p.Met156=
ENST00000616066.4:c.544A=	ENSP00000485000.1:p.Met182=
ENST00000622390.4:c.655A=	ENSP00000477503.1:p.Met219=
NM_001039847.2:c.569A=	NP_001034936.1:p.His190=
NM_001039848.2:c.658A=	NP_001034937.1:p.Met220=
NM_002085.4:c.547A=	NP_002076.2:p.Met183=
NM_001039848.3:c.658A=	NP_001034937.1:p.Met220=
NM_001039847.3:c.569A=	NP_001034936.1:p.His190=
NM_001039848.4:c.658A=	NP_001034937.1:p.Met220=
NM_001367832.1:c.466A=	NP_001354761.1:p.Met156=
NM_002085.5:c.547A= MANE Select	NP_002076.2:p.Met183=