Canonical Allele Identifier: CA2317520517

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106244C= , CM000681.2:g.1106244C=	GRCh38
NC_000019.9:g.1106243C= , CM000681.1:g.1106243C=	GRCh37
NC_000019.8:g.1057243C=	NCBI36
NG_050621.1:g.7319C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.590C=	ENSP00000473614.3:p.Ala197=
ENST00000593032.6:c.459C=	ENSP00000465828.4:p.Cys153=
ENST00000706713.1:c.473C=	ENSP00000516510.1:p.Ala158=
ENST00000706714.1:c.459C=	ENSP00000516511.1:p.Cys153=
ENST00000706715.1:c.95C=	ENSP00000516512.1:p.Ala32=
ENST00000354171.13:c.479C= MANE Select	ENSP00000346103.7:p.Ala160=
ENST00000589115.6:c.477-156C=	ENSP00000466872.3:n.477-156C=
ENST00000354171.12:c.479C=	ENSP00000346103.7:p.Ala160=
ENST00000585480.1:c.212C=	ENSP00000467900.1:p.Ala71=
ENST00000587648.5:c.359C=	ENSP00000468349.1:p.Ala120=
ENST00000588919.5:c.398C=	ENSP00000464989.3:p.Ala133=
ENST00000589115.5:c.477-156C=	ENSP00000466872.2:n.477-156C=
ENST00000592940.2:n.850C=
ENST00000593032.5:c.459C=	ENSP00000465828.3:p.Cys153=
ENST00000611653.4:c.398C=	ENSP00000483655.1:p.Ala133=
ENST00000616066.4:c.476C=	ENSP00000485000.1:p.Ala159=
ENST00000622390.4:c.587C=	ENSP00000477503.1:p.Ala196=
NM_001039847.2:c.479C=	NP_001034936.1:p.Ala160=
NM_001039848.2:c.590C=	NP_001034937.1:p.Ala197=
NM_002085.4:c.479C=	NP_002076.2:p.Ala160=
NM_001039848.3:c.590C=	NP_001034937.1:p.Ala197=
NM_001039847.3:c.479C=	NP_001034936.1:p.Ala160=
NM_001039848.4:c.590C=	NP_001034937.1:p.Ala197=
NM_001367832.1:c.398C=	NP_001354761.1:p.Ala133=
NM_002085.5:c.479C= MANE Select	NP_002076.2:p.Ala160=