Canonical Allele Identifier: CA402939131

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106246T>G (hg19) ; chr19:g.1106247T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106247T>G , CM000681.2:g.1106247T>G	GRCh38
NC_000019.9:g.1106246T>G , CM000681.1:g.1106246T>G	GRCh37
NC_000019.8:g.1057246T>G	NCBI36
NG_050621.1:g.7322T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.593T>G	ENSP00000473614.3:p.Ile198Ser
ENST00000593032.6:c.462T>G	ENSP00000465828.4:p.His154Gln
ENST00000706713.1:c.476T>G	ENSP00000516510.1:p.Ile159Ser
ENST00000706714.1:c.462T>G	ENSP00000516511.1:p.His154Gln
ENST00000706715.1:c.98T>G	ENSP00000516512.1:p.Ile33Ser
ENST00000354171.13:c.482T>G MANE Select	ENSP00000346103.7:p.Ile161Ser
ENST00000589115.6:c.477-153T>G	ENSP00000466872.3:n.477-153T>G
ENST00000354171.12:c.482T>G	ENSP00000346103.7:p.Ile161Ser
ENST00000585480.1:c.215T>G	ENSP00000467900.1:p.Ile72Ser
ENST00000587648.5:c.362T>G	ENSP00000468349.1:p.Ile121Ser
ENST00000588919.5:c.401T>G	ENSP00000464989.3:p.Ile134Ser
ENST00000589115.5:c.477-153T>G	ENSP00000466872.2:n.477-153T>G
ENST00000592940.2:n.853T>G
ENST00000593032.5:c.462T>G	ENSP00000465828.3:p.His154Gln
ENST00000611653.4:c.401T>G	ENSP00000483655.1:p.Ile134Ser
ENST00000616066.4:c.479T>G	ENSP00000485000.1:p.Ile160Ser
ENST00000622390.4:c.590T>G	ENSP00000477503.1:p.Ile197Ser
NM_001039847.2:c.482T>G	NP_001034936.1:p.Ile161Ser
NM_001039848.2:c.593T>G	NP_001034937.1:p.Ile198Ser
NM_002085.4:c.482T>G	NP_002076.2:p.Ile161Ser
NM_001039848.3:c.593T>G	NP_001034937.1:p.Ile198Ser
NM_001039847.3:c.482T>G	NP_001034936.1:p.Ile161Ser
NM_001039848.4:c.593T>G	NP_001034937.1:p.Ile198Ser
NM_001367832.1:c.401T>G	NP_001354761.1:p.Ile134Ser
NM_002085.5:c.482T>G MANE Select	NP_002076.2:p.Ile161Ser