Canonical Allele Identifier: CA402939608

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106399T>A (hg19) ; chr19:g.1106400T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106400T>A , CM000681.2:g.1106400T>A	GRCh38
NC_000019.9:g.1106399T>A , CM000681.1:g.1106399T>A	GRCh37
NC_000019.8:g.1057399T>A	NCBI36
NG_050621.1:g.7475T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.613T>A	ENSP00000473614.3:p.Phe205Ile
ENST00000593032.6:c.482T>A	ENSP00000465828.4:p.Val161Asp
ENST00000706713.1:c.496T>A	ENSP00000516510.1:p.Phe166Ile
ENST00000706714.1:c.482T>A	ENSP00000516511.1:p.Val161Asp
ENST00000706715.1:c.118T>A	ENSP00000516512.1:p.Phe40Ile
ENST00000354171.13:c.502T>A MANE Select	ENSP00000346103.7:p.Phe168Ile
ENST00000589115.6:c.477T>A	ENSP00000466872.3:p.Asn159Lys
ENST00000354171.12:c.502T>A	ENSP00000346103.7:p.Phe168Ile
ENST00000585480.1:c.235T>A	ENSP00000467900.1:p.Phe79Ile
ENST00000587648.5:c.382T>A	ENSP00000468349.1:p.Phe128Ile
ENST00000588919.5:c.443T>A	ENSP00000464989.3:p.Val148Asp
ENST00000589115.5:c.477T>A	ENSP00000466872.2:p.Asn159Lys
ENST00000592940.2:n.873T>A
ENST00000593032.5:c.482T>A	ENSP00000465828.3:p.Val161Asp
ENST00000611653.4:c.421T>A	ENSP00000483655.1:p.Phe141Ile
ENST00000616066.4:c.499T>A	ENSP00000485000.1:p.Phe167Ile
ENST00000622390.4:c.610T>A	ENSP00000477503.1:p.Phe204Ile
NM_001039847.2:c.524T>A	NP_001034936.1:p.Val175Asp
NM_001039848.2:c.613T>A	NP_001034937.1:p.Phe205Ile
NM_002085.4:c.502T>A	NP_002076.2:p.Phe168Ile
NM_001039848.3:c.613T>A	NP_001034937.1:p.Phe205Ile
NM_001039847.3:c.524T>A	NP_001034936.1:p.Val175Asp
NM_001039848.4:c.613T>A	NP_001034937.1:p.Phe205Ile
NM_001367832.1:c.421T>A	NP_001354761.1:p.Phe141Ile
NM_002085.5:c.502T>A MANE Select	NP_002076.2:p.Phe168Ile