Canonical Allele Identifier: CA2317520428

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106126T= , CM000681.2:g.1106126T=	GRCh38
NC_000019.9:g.1106125T= , CM000681.1:g.1106125T=	GRCh37
NC_000019.8:g.1057125T=	NCBI36
NG_050621.1:g.7201T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-116T=	ENSP00000473614.3:n.588-116T=
ENST00000593032.6:c.396-55T=	ENSP00000465828.4:n.396-55T=
ENST00000706713.1:c.471-116T=	ENSP00000516510.1:n.471-116T=
ENST00000706714.1:c.396-55T=	ENSP00000516511.1:n.396-55T=
ENST00000706715.1:c.93-116T=	ENSP00000516512.1:n.93-116T=
ENST00000354171.13:c.477-116T= MANE Select	ENSP00000346103.7:n.477-116T=
ENST00000589115.6:c.477-274T=	ENSP00000466872.3:n.477-274T=
ENST00000354171.12:c.477-116T=	ENSP00000346103.7:n.477-116T=
ENST00000585480.1:c.210-116T=	ENSP00000467900.1:n.210-116T=
ENST00000587648.5:c.357-116T=	ENSP00000468349.1:n.357-116T=
ENST00000588919.5:c.396-116T=	ENSP00000464989.3:n.396-116T=
ENST00000589115.5:c.477-274T=	ENSP00000466872.2:n.477-274T=
ENST00000592940.2:n.732T=
ENST00000593032.5:c.396-55T=	ENSP00000465828.3:n.396-55T=
ENST00000611653.4:c.396-116T=	ENSP00000483655.1:n.396-116T=
ENST00000616066.4:c.474-116T=	ENSP00000485000.1:n.474-116T=
ENST00000622390.4:c.585-116T=	ENSP00000477503.1:n.585-116T=
NM_001039847.2:c.477-116T=	NP_001034936.1:n.477-116T=
NM_001039848.2:c.588-116T=	NP_001034937.1:n.588-116T=
NM_002085.4:c.477-116T=	NP_002076.2:n.477-116T=
NM_001039848.3:c.588-116T=	NP_001034937.1:n.588-116T=
NM_001039847.3:c.477-116T=	NP_001034936.1:n.477-116T=
NM_001039848.4:c.588-116T=	NP_001034937.1:n.588-116T=
NM_001367832.1:c.396-116T=	NP_001354761.1:n.396-116T=
NM_002085.5:c.477-116T= MANE Select	NP_002076.2:n.477-116T=