Canonical Allele Identifier: CA2317520109

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105731T= , CM000681.2:g.1105731T=	GRCh38
NC_000019.9:g.1105730T= , CM000681.1:g.1105730T=	GRCh37
NC_000019.8:g.1056730T=	NCBI36
NG_050621.1:g.6806T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.509T=	ENSP00000473614.3:p.Ile170=
ENST00000593032.6:c.317T=	ENSP00000465828.4:p.Ile106=
ENST00000706713.1:c.392T=	ENSP00000516510.1:p.Ile131=
ENST00000706714.1:c.317T=	ENSP00000516511.1:p.Ile106=
ENST00000706715.1:c.14T=	ENSP00000516512.1:p.Ile5=
ENST00000354171.13:c.398T= MANE Select	ENSP00000346103.7:p.Ile133=
ENST00000589115.6:c.398T=	ENSP00000466872.3:p.Ile133=
ENST00000354171.12:c.398T=	ENSP00000346103.7:p.Ile133=
ENST00000585362.6:c.509T=	ENSP00000473614.2:p.Ile170=
ENST00000585480.1:c.131T=	ENSP00000467900.1:p.Ile44=
ENST00000587648.5:c.278T=	ENSP00000468349.1:p.Ile93=
ENST00000588919.5:c.317T=	ENSP00000464989.3:p.Ile106=
ENST00000589115.5:c.398T=	ENSP00000466872.2:p.Ile133=
ENST00000592940.2:n.337T=
ENST00000593032.5:c.317T=	ENSP00000465828.3:p.Ile106=
ENST00000611653.4:c.317T=	ENSP00000483655.1:p.Ile106=
ENST00000616066.4:c.395T=	ENSP00000485000.1:p.Ile132=
ENST00000622390.4:c.506T=	ENSP00000477503.1:p.Ile169=
NM_001039847.2:c.398T=	NP_001034936.1:p.Ile133=
NM_001039848.2:c.509T=	NP_001034937.1:p.Ile170=
NM_002085.4:c.398T=	NP_002076.2:p.Ile133=
NM_001039848.3:c.509T=	NP_001034937.1:p.Ile170=
NM_001039847.3:c.398T=	NP_001034936.1:p.Ile133=
NM_001039848.4:c.509T=	NP_001034937.1:p.Ile170=
NM_001367832.1:c.317T=	NP_001354761.1:p.Ile106=
NM_002085.5:c.398T= MANE Select	NP_002076.2:p.Ile133=