Canonical Allele Identifier: CA402939621

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106400T>A (hg19) ; chr19:g.1106401T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106401T>A , CM000681.2:g.1106401T>A	GRCh38
NC_000019.9:g.1106400T>A , CM000681.1:g.1106400T>A	GRCh37
NC_000019.8:g.1057400T>A	NCBI36
NG_050621.1:g.7476T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.614T>A	ENSP00000473614.3:p.Phe205Tyr
ENST00000593032.6:c.483T>A	ENSP00000465828.4:p.Val161=
ENST00000706713.1:c.497T>A	ENSP00000516510.1:p.Phe166Tyr
ENST00000706714.1:c.483T>A	ENSP00000516511.1:p.Val161=
ENST00000706715.1:c.119T>A	ENSP00000516512.1:p.Phe40Tyr
ENST00000354171.13:c.503T>A MANE Select	ENSP00000346103.7:p.Phe168Tyr
ENST00000589115.6:c.478T>A	ENSP00000466872.3:p.Ser160Thr
ENST00000354171.12:c.503T>A	ENSP00000346103.7:p.Phe168Tyr
ENST00000585480.1:c.236T>A	ENSP00000467900.1:p.Phe79Tyr
ENST00000587648.5:c.383T>A	ENSP00000468349.1:p.Phe128Tyr
ENST00000588919.5:c.444T>A	ENSP00000464989.3:p.Val148=
ENST00000589115.5:c.478T>A	ENSP00000466872.2:p.Ser160Thr
ENST00000592940.2:n.874T>A
ENST00000593032.5:c.483T>A	ENSP00000465828.3:p.Val161=
ENST00000611653.4:c.422T>A	ENSP00000483655.1:p.Phe141Tyr
ENST00000616066.4:c.500T>A	ENSP00000485000.1:p.Phe167Tyr
ENST00000622390.4:c.611T>A	ENSP00000477503.1:p.Phe204Tyr
NM_001039847.2:c.525T>A	NP_001034936.1:p.Val175=
NM_001039848.2:c.614T>A	NP_001034937.1:p.Phe205Tyr
NM_002085.4:c.503T>A	NP_002076.2:p.Phe168Tyr
NM_001039848.3:c.614T>A	NP_001034937.1:p.Phe205Tyr
NM_001039847.3:c.525T>A	NP_001034936.1:p.Val175=
NM_001039848.4:c.614T>A	NP_001034937.1:p.Phe205Tyr
NM_001367832.1:c.422T>A	NP_001354761.1:p.Phe141Tyr
NM_002085.5:c.503T>A MANE Select	NP_002076.2:p.Phe168Tyr