Canonical Allele Identifier: CA2317520676

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106457C= , CM000681.2:g.1106457C=	GRCh38
NC_000019.9:g.1106456C= , CM000681.1:g.1106456C=	GRCh37
NC_000019.8:g.1057456C=	NCBI36
NG_050621.1:g.7532C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.670C=	ENSP00000473614.3:p.Leu224=
ENST00000593032.6:c.539C=	ENSP00000465828.4:p.Pro180=
ENST00000706713.1:c.553C=	ENSP00000516510.1:p.Leu185=
ENST00000706714.1:c.539C=	ENSP00000516511.1:p.Pro180=
ENST00000706715.1:c.175C=	ENSP00000516512.1:p.Leu59=
ENST00000354171.13:c.559C= MANE Select	ENSP00000346103.7:p.Leu187=
ENST00000589115.6:c.534C=	ENSP00000466872.3:p.Pro178=
ENST00000354171.12:c.559C=	ENSP00000346103.7:p.Leu187=
ENST00000585480.1:c.292C=	ENSP00000467900.1:p.Leu98=
ENST00000587648.5:c.439C=	ENSP00000468349.1:p.Leu147=
ENST00000588919.5:c.500C=	ENSP00000464989.3:p.Pro167=
ENST00000589115.5:c.534C=	ENSP00000466872.2:p.Pro178=
ENST00000592940.2:n.930C=
ENST00000611653.4:c.478C=	ENSP00000483655.1:p.Leu160=
ENST00000616066.4:c.556C=	ENSP00000485000.1:p.Leu186=
ENST00000622390.4:c.667C=	ENSP00000477503.1:p.Leu223=
NM_001039847.2:c.581C=	NP_001034936.1:p.Pro194=
NM_001039848.2:c.670C=	NP_001034937.1:p.Leu224=
NM_002085.4:c.559C=	NP_002076.2:p.Leu187=
NM_001039848.3:c.670C=	NP_001034937.1:p.Leu224=
NM_001039847.3:c.581C=	NP_001034936.1:p.Pro194=
NM_001039848.4:c.670C=	NP_001034937.1:p.Leu224=
NM_001367832.1:c.478C=	NP_001354761.1:p.Leu160=
NM_002085.5:c.559C= MANE Select	NP_002076.2:p.Leu187=