Canonical Allele Identifier: CA2317520124

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105753C= , CM000681.2:g.1105753C=	GRCh38
NC_000019.9:g.1105752C= , CM000681.1:g.1105752C=	GRCh37
NC_000019.8:g.1056752C=	NCBI36
NG_050621.1:g.6828C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.531C=	ENSP00000473614.3:p.Ala177=
ENST00000593032.6:c.339C=	ENSP00000465828.4:p.Ala113=
ENST00000706713.1:c.414C=	ENSP00000516510.1:p.Ala138=
ENST00000706714.1:c.339C=	ENSP00000516511.1:p.Ala113=
ENST00000706715.1:c.36C=	ENSP00000516512.1:p.Ala12=
ENST00000354171.13:c.420C= MANE Select	ENSP00000346103.7:p.Ala140=
ENST00000589115.6:c.420C=	ENSP00000466872.3:p.Ala140=
ENST00000354171.12:c.420C=	ENSP00000346103.7:p.Ala140=
ENST00000585362.6:c.531C=	ENSP00000473614.2:p.Ala177=
ENST00000585480.1:c.153C=	ENSP00000467900.1:p.Ala51=
ENST00000587648.5:c.300C=	ENSP00000468349.1:p.Ala100=
ENST00000588919.5:c.339C=	ENSP00000464989.3:p.Ala113=
ENST00000589115.5:c.420C=	ENSP00000466872.2:p.Ala140=
ENST00000592940.2:n.359C=
ENST00000593032.5:c.339C=	ENSP00000465828.3:p.Ala113=
ENST00000611653.4:c.339C=	ENSP00000483655.1:p.Ala113=
ENST00000616066.4:c.417C=	ENSP00000485000.1:p.Ala139=
ENST00000622390.4:c.528C=	ENSP00000477503.1:p.Ala176=
NM_001039847.2:c.420C=	NP_001034936.1:p.Ala140=
NM_001039848.2:c.531C=	NP_001034937.1:p.Ala177=
NM_002085.4:c.420C=	NP_002076.2:p.Ala140=
NM_001039848.3:c.531C=	NP_001034937.1:p.Ala177=
NM_001039847.3:c.420C=	NP_001034936.1:p.Ala140=
NM_001039848.4:c.531C=	NP_001034937.1:p.Ala177=
NM_001367832.1:c.339C=	NP_001354761.1:p.Ala113=
NM_002085.5:c.420C= MANE Select	NP_002076.2:p.Ala140=