Canonical Allele Identifier: CA2317519917

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105456C= , CM000681.2:g.1105456C=	GRCh38
NC_000019.9:g.1105455C= , CM000681.1:g.1105455C=	GRCh37
NC_000019.8:g.1056455C=	NCBI36
NG_050621.1:g.6531C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002085.5:c.270C= MANE Select	NP_002076.2:p.Tyr90=
ENST00000354171.13:c.270C= MANE Select	ENSP00000346103.7:p.Tyr90=
NM_001039847.2:c.270C=	NP_001034936.1:p.Tyr90=
NM_001039847.3:c.270C=	NP_001034936.1:p.Tyr90=
NM_001039848.2:c.381C=	NP_001034937.1:p.Tyr127=
NM_001039848.3:c.381C=	NP_001034937.1:p.Tyr127=
NM_001039848.4:c.381C=	NP_001034937.1:p.Tyr127=
NM_001367832.1:c.189C=	NP_001354761.1:p.Tyr63=
NM_002085.4:c.270C=	NP_002076.2:p.Tyr90=
ENST00000354171.12:c.270C=	ENSP00000346103.7:p.Tyr90=
ENST00000585362.6:c.381C=	ENSP00000473614.2:p.Tyr127=
ENST00000585362.7:c.381C=	ENSP00000473614.3:p.Tyr127=
ENST00000585480.1:c.3C=	ENSP00000467900.1:p.Tyr1=
ENST00000587648.5:c.150C=	ENSP00000468349.1:p.Tyr50=
ENST00000587932.2:n.204C=
ENST00000588919.5:c.189C=	ENSP00000464989.3:p.Tyr63=
ENST00000589115.5:c.270C=	ENSP00000466872.2:p.Tyr90=
ENST00000589115.6:c.270C=	ENSP00000466872.3:p.Tyr90=
ENST00000592940.2:n.216C=
ENST00000593032.5:c.189C=	ENSP00000465828.3:p.Tyr63=
ENST00000593032.6:c.189C=	ENSP00000465828.4:p.Tyr63=
ENST00000611653.4:c.189C=	ENSP00000483655.1:p.Tyr63=
ENST00000614791.1:c.375C=	ENSP00000484697.1:p.Tyr125=
ENST00000616066.4:c.267C=	ENSP00000485000.1:p.Tyr89=
ENST00000622390.4:c.378C=	ENSP00000477503.1:p.Tyr126=
ENST00000706713.1:c.264C=	ENSP00000516510.1:p.Tyr88=
ENST00000706714.1:c.189C=	ENSP00000516511.1:p.Tyr63=
ENST00000706715.1:c.-115C=	ENSP00000516512.1:n.-115C=