Canonical Allele Identifier: CA2317520675

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106456C= , CM000681.2:g.1106456C=	GRCh38
NC_000019.9:g.1106455C= , CM000681.1:g.1106455C=	GRCh37
NC_000019.8:g.1057455C=	NCBI36
NG_050621.1:g.7531C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.669C=	ENSP00000473614.3:p.Pro223=
ENST00000593032.6:c.538C=	ENSP00000465828.4:p.Pro180=
ENST00000706713.1:c.552C=	ENSP00000516510.1:p.Pro184=
ENST00000706714.1:c.538C=	ENSP00000516511.1:p.Pro180=
ENST00000706715.1:c.174C=	ENSP00000516512.1:p.Pro58=
ENST00000354171.13:c.558C= MANE Select	ENSP00000346103.7:p.Pro186=
ENST00000589115.6:c.533C=	ENSP00000466872.3:p.Pro178=
ENST00000354171.12:c.558C=	ENSP00000346103.7:p.Pro186=
ENST00000585480.1:c.291C=	ENSP00000467900.1:p.Pro97=
ENST00000587648.5:c.438C=	ENSP00000468349.1:p.Pro146=
ENST00000588919.5:c.499C=	ENSP00000464989.3:p.Pro167=
ENST00000589115.5:c.533C=	ENSP00000466872.2:p.Pro178=
ENST00000592940.2:n.929C=
ENST00000611653.4:c.477C=	ENSP00000483655.1:p.Pro159=
ENST00000616066.4:c.555C=	ENSP00000485000.1:p.Pro185=
ENST00000622390.4:c.666C=	ENSP00000477503.1:p.Pro222=
NM_001039847.2:c.580C=	NP_001034936.1:p.Pro194=
NM_001039848.2:c.669C=	NP_001034937.1:p.Pro223=
NM_002085.4:c.558C=	NP_002076.2:p.Pro186=
NM_001039848.3:c.669C=	NP_001034937.1:p.Pro223=
NM_001039847.3:c.580C=	NP_001034936.1:p.Pro194=
NM_001039848.4:c.669C=	NP_001034937.1:p.Pro223=
NM_001367832.1:c.477C=	NP_001354761.1:p.Pro159=
NM_002085.5:c.558C= MANE Select	NP_002076.2:p.Pro186=