Canonical Allele Identifier: CA2317520667

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106442C= , CM000681.2:g.1106442C=	GRCh38
NC_000019.9:g.1106441C= , CM000681.1:g.1106441C=	GRCh37
NC_000019.8:g.1057441C=	NCBI36
NG_050621.1:g.7517C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.655C=	ENSP00000473614.3:p.Pro219=
ENST00000593032.6:c.524C=	ENSP00000465828.4:p.Thr175=
ENST00000706713.1:c.538C=	ENSP00000516510.1:p.Pro180=
ENST00000706714.1:c.524C=	ENSP00000516511.1:p.Thr175=
ENST00000706715.1:c.160C=	ENSP00000516512.1:p.Pro54=
ENST00000354171.13:c.544C= MANE Select	ENSP00000346103.7:p.Pro182=
ENST00000589115.6:c.519C=	ENSP00000466872.3:p.Asp173=
ENST00000354171.12:c.544C=	ENSP00000346103.7:p.Pro182=
ENST00000585480.1:c.277C=	ENSP00000467900.1:p.Pro93=
ENST00000587648.5:c.424C=	ENSP00000468349.1:p.Pro142=
ENST00000588919.5:c.485C=	ENSP00000464989.3:p.Thr162=
ENST00000589115.5:c.519C=	ENSP00000466872.2:p.Asp173=
ENST00000592940.2:n.915C=
ENST00000593032.5:c.524C=	ENSP00000465828.3:p.Thr175=
ENST00000611653.4:c.463C=	ENSP00000483655.1:p.Pro155=
ENST00000616066.4:c.541C=	ENSP00000485000.1:p.Pro181=
ENST00000622390.4:c.652C=	ENSP00000477503.1:p.Pro218=
NM_001039847.2:c.566C=	NP_001034936.1:p.Thr189=
NM_001039848.2:c.655C=	NP_001034937.1:p.Pro219=
NM_002085.4:c.544C=	NP_002076.2:p.Pro182=
NM_001039848.3:c.655C=	NP_001034937.1:p.Pro219=
NM_001039847.3:c.566C=	NP_001034936.1:p.Thr189=
NM_001039848.4:c.655C=	NP_001034937.1:p.Pro219=
NM_001367832.1:c.463C=	NP_001354761.1:p.Pro155=
NM_002085.5:c.544C= MANE Select	NP_002076.2:p.Pro182=