Canonical Allele Identifier: CA2317520097

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105706G= , CM000681.2:g.1105706G=	GRCh38
NC_000019.9:g.1105705G= , CM000681.1:g.1105705G=	GRCh37
NC_000019.8:g.1056705G=	NCBI36
NG_050621.1:g.6781G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.484G=	ENSP00000473614.3:p.Val162=
ENST00000593032.6:c.292G=	ENSP00000465828.4:p.Val98=
ENST00000706713.1:c.367G=	ENSP00000516510.1:p.Val123=
ENST00000706714.1:c.292G=	ENSP00000516511.1:p.Val98=
ENST00000706715.1:c.-12G=	ENSP00000516512.1:n.-12G=
ENST00000354171.13:c.373G= MANE Select	ENSP00000346103.7:p.Val125=
ENST00000589115.6:c.373G=	ENSP00000466872.3:p.Val125=
ENST00000354171.12:c.373G=	ENSP00000346103.7:p.Val125=
ENST00000585362.6:c.484G=	ENSP00000473614.2:p.Val162=
ENST00000585480.1:c.106G=	ENSP00000467900.1:p.Val36=
ENST00000587648.5:c.253G=	ENSP00000468349.1:p.Val85=
ENST00000588919.5:c.292G=	ENSP00000464989.3:p.Val98=
ENST00000589115.5:c.373G=	ENSP00000466872.2:p.Val125=
ENST00000592940.2:n.312G=
ENST00000593032.5:c.292G=	ENSP00000465828.3:p.Val98=
ENST00000611653.4:c.292G=	ENSP00000483655.1:p.Val98=
ENST00000616066.4:c.370G=	ENSP00000485000.1:p.Val124=
ENST00000622390.4:c.481G=	ENSP00000477503.1:p.Val161=
NM_001039847.2:c.373G=	NP_001034936.1:p.Val125=
NM_001039848.2:c.484G=	NP_001034937.1:p.Val162=
NM_002085.4:c.373G=	NP_002076.2:p.Val125=
NM_001039848.3:c.484G=	NP_001034937.1:p.Val162=
NM_001039847.3:c.373G=	NP_001034936.1:p.Val125=
NM_001039848.4:c.484G=	NP_001034937.1:p.Val162=
NM_001367832.1:c.292G=	NP_001354761.1:p.Val98=
NM_002085.5:c.373G= MANE Select	NP_002076.2:p.Val125=