Canonical Allele Identifier: CA402939226

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106259C>G (hg19) ; chr19:g.1106260C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106260C>G , CM000681.2:g.1106260C>G	GRCh38
NC_000019.9:g.1106259C>G , CM000681.1:g.1106259C>G	GRCh37
NC_000019.8:g.1057259C>G	NCBI36
NG_050621.1:g.7335C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.606C>G	ENSP00000473614.3:p.Phe202Leu
ENST00000593032.6:c.475C>G	ENSP00000465828.4:p.His159Asp
ENST00000706713.1:c.489C>G	ENSP00000516510.1:p.Phe163Leu
ENST00000706714.1:c.475C>G	ENSP00000516511.1:p.His159Asp
ENST00000706715.1:c.111C>G	ENSP00000516512.1:p.Phe37Leu
ENST00000354171.13:c.495C>G MANE Select	ENSP00000346103.7:p.Phe165Leu
ENST00000589115.6:c.477-140C>G	ENSP00000466872.3:n.477-140C>G
ENST00000354171.12:c.495C>G	ENSP00000346103.7:p.Phe165Leu
ENST00000585480.1:c.228C>G	ENSP00000467900.1:p.Phe76Leu
ENST00000587648.5:c.375C>G	ENSP00000468349.1:p.Phe125Leu
ENST00000588919.5:c.414C>G	ENSP00000464989.3:p.Phe138Leu
ENST00000589115.5:c.477-140C>G	ENSP00000466872.2:n.477-140C>G
ENST00000592940.2:n.866C>G
ENST00000593032.5:c.475C>G	ENSP00000465828.3:p.His159Asp
ENST00000611653.4:c.414C>G	ENSP00000483655.1:p.Phe138Leu
ENST00000616066.4:c.492C>G	ENSP00000485000.1:p.Phe164Leu
ENST00000622390.4:c.603C>G	ENSP00000477503.1:p.Phe201Leu
NM_001039847.2:c.495C>G	NP_001034936.1:p.Phe165Leu
NM_001039848.2:c.606C>G	NP_001034937.1:p.Phe202Leu
NM_002085.4:c.495C>G	NP_002076.2:p.Phe165Leu
NM_001039848.3:c.606C>G	NP_001034937.1:p.Phe202Leu
NM_001039847.3:c.495C>G	NP_001034936.1:p.Phe165Leu
NM_001039848.4:c.606C>G	NP_001034937.1:p.Phe202Leu
NM_001367832.1:c.414C>G	NP_001354761.1:p.Phe138Leu
NM_002085.5:c.495C>G MANE Select	NP_002076.2:p.Phe165Leu