Canonical Allele Identifier: CA402940162

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106453C>G (hg19) ; chr19:g.1106454C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106454C>G , CM000681.2:g.1106454C>G	GRCh38
NC_000019.9:g.1106453C>G , CM000681.1:g.1106453C>G	GRCh37
NC_000019.8:g.1057453C>G	NCBI36
NG_050621.1:g.7529C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.667C>G	ENSP00000473614.3:p.Pro223Ala
ENST00000593032.6:c.536C>G	ENSP00000465828.4:p.Ala179Gly
ENST00000706713.1:c.550C>G	ENSP00000516510.1:p.Pro184Ala
ENST00000706714.1:c.536C>G	ENSP00000516511.1:p.Ala179Gly
ENST00000706715.1:c.172C>G	ENSP00000516512.1:p.Pro58Ala
ENST00000354171.13:c.556C>G MANE Select	ENSP00000346103.7:p.Pro186Ala
ENST00000589115.6:c.531C>G	ENSP00000466872.3:p.Ser177Arg
ENST00000354171.12:c.556C>G	ENSP00000346103.7:p.Pro186Ala
ENST00000585480.1:c.289C>G	ENSP00000467900.1:p.Pro97Ala
ENST00000587648.5:c.436C>G	ENSP00000468349.1:p.Pro146Ala
ENST00000588919.5:c.497C>G	ENSP00000464989.3:p.Ala166Gly
ENST00000589115.5:c.531C>G	ENSP00000466872.2:p.Ser177Arg
ENST00000592940.2:n.927C>G
ENST00000611653.4:c.475C>G	ENSP00000483655.1:p.Pro159Ala
ENST00000616066.4:c.553C>G	ENSP00000485000.1:p.Pro185Ala
ENST00000622390.4:c.664C>G	ENSP00000477503.1:p.Pro222Ala
NM_001039847.2:c.578C>G	NP_001034936.1:p.Ala193Gly
NM_001039848.2:c.667C>G	NP_001034937.1:p.Pro223Ala
NM_002085.4:c.556C>G	NP_002076.2:p.Pro186Ala
NM_001039848.3:c.667C>G	NP_001034937.1:p.Pro223Ala
NM_001039847.3:c.578C>G	NP_001034936.1:p.Ala193Gly
NM_001039848.4:c.667C>G	NP_001034937.1:p.Pro223Ala
NM_001367832.1:c.475C>G	NP_001354761.1:p.Pro159Ala
NM_002085.5:c.556C>G MANE Select	NP_002076.2:p.Pro186Ala