Canonical Allele Identifier: CA402939837

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106414A>T (hg19) ; chr19:g.1106415A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106415A>T , CM000681.2:g.1106415A>T	GRCh38
NC_000019.9:g.1106414A>T , CM000681.1:g.1106414A>T	GRCh37
NC_000019.8:g.1057414A>T	NCBI36
NG_050621.1:g.7490A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.628A>T	ENSP00000473614.3:p.Asn210Tyr
ENST00000593032.6:c.497A>T	ENSP00000465828.4:p.Glu166Val
ENST00000706713.1:c.511A>T	ENSP00000516510.1:p.Asn171Tyr
ENST00000706714.1:c.497A>T	ENSP00000516511.1:p.Glu166Val
ENST00000706715.1:c.133A>T	ENSP00000516512.1:p.Asn45Tyr
ENST00000354171.13:c.517A>T MANE Select	ENSP00000346103.7:p.Asn173Tyr
ENST00000589115.6:c.492A>T	ENSP00000466872.3:p.Arg164Ser
ENST00000354171.12:c.517A>T	ENSP00000346103.7:p.Asn173Tyr
ENST00000585480.1:c.250A>T	ENSP00000467900.1:p.Asn84Tyr
ENST00000587648.5:c.397A>T	ENSP00000468349.1:p.Asn133Tyr
ENST00000588919.5:c.458A>T	ENSP00000464989.3:p.Glu153Val
ENST00000589115.5:c.492A>T	ENSP00000466872.2:p.Arg164Ser
ENST00000592940.2:n.888A>T
ENST00000593032.5:c.497A>T	ENSP00000465828.3:p.Glu166Val
ENST00000611653.4:c.436A>T	ENSP00000483655.1:p.Asn146Tyr
ENST00000616066.4:c.514A>T	ENSP00000485000.1:p.Asn172Tyr
ENST00000622390.4:c.625A>T	ENSP00000477503.1:p.Asn209Tyr
NM_001039847.2:c.539A>T	NP_001034936.1:p.Glu180Val
NM_001039848.2:c.628A>T	NP_001034937.1:p.Asn210Tyr
NM_002085.4:c.517A>T	NP_002076.2:p.Asn173Tyr
NM_001039848.3:c.628A>T	NP_001034937.1:p.Asn210Tyr
NM_001039847.3:c.539A>T	NP_001034936.1:p.Glu180Val
NM_001039848.4:c.628A>T	NP_001034937.1:p.Asn210Tyr
NM_001367832.1:c.436A>T	NP_001354761.1:p.Asn146Tyr
NM_002085.5:c.517A>T MANE Select	NP_002076.2:p.Asn173Tyr