Canonical Allele Identifier: CA2317520133

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105777G= , CM000681.2:g.1105777G=	GRCh38
NC_000019.9:g.1105776G= , CM000681.1:g.1105776G=	GRCh37
NC_000019.8:g.1056776G=	NCBI36
NG_050621.1:g.6852G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.555G=	ENSP00000473614.3:p.Lys185=
ENST00000593032.6:c.363G=	ENSP00000465828.4:p.Lys121=
ENST00000706713.1:c.438G=	ENSP00000516510.1:p.Lys146=
ENST00000706714.1:c.363G=	ENSP00000516511.1:p.Lys121=
ENST00000706715.1:c.60G=	ENSP00000516512.1:p.Lys20=
ENST00000354171.13:c.444G= MANE Select	ENSP00000346103.7:p.Lys148=
ENST00000589115.6:c.444G=	ENSP00000466872.3:p.Lys148=
ENST00000354171.12:c.444G=	ENSP00000346103.7:p.Lys148=
ENST00000585480.1:c.177G=	ENSP00000467900.1:p.Lys59=
ENST00000587648.5:c.324G=	ENSP00000468349.1:p.Lys108=
ENST00000588919.5:c.363G=	ENSP00000464989.3:p.Lys121=
ENST00000589115.5:c.444G=	ENSP00000466872.2:p.Lys148=
ENST00000592940.2:n.383G=
ENST00000593032.5:c.363G=	ENSP00000465828.3:p.Lys121=
ENST00000611653.4:c.363G=	ENSP00000483655.1:p.Lys121=
ENST00000616066.4:c.441G=	ENSP00000485000.1:p.Lys147=
ENST00000622390.4:c.552G=	ENSP00000477503.1:p.Lys184=
NM_001039847.2:c.444G=	NP_001034936.1:p.Lys148=
NM_001039848.2:c.555G=	NP_001034937.1:p.Lys185=
NM_002085.4:c.444G=	NP_002076.2:p.Lys148=
NM_001039848.3:c.555G=	NP_001034937.1:p.Lys185=
NM_001039847.3:c.444G=	NP_001034936.1:p.Lys148=
NM_001039848.4:c.555G=	NP_001034937.1:p.Lys185=
NM_001367832.1:c.363G=	NP_001354761.1:p.Lys121=
NM_002085.5:c.444G= MANE Select	NP_002076.2:p.Lys148=