Canonical Allele Identifier: CA402940137

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106450G>T (hg19) ; chr19:g.1106451G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106451G>T , CM000681.2:g.1106451G>T	GRCh38
NC_000019.9:g.1106450G>T , CM000681.1:g.1106450G>T	GRCh37
NC_000019.8:g.1057450G>T	NCBI36
NG_050621.1:g.7526G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.664G>T	ENSP00000473614.3:p.Glu222Ter
ENST00000593032.6:c.533G>T	ENSP00000465828.4:p.Gly178Val
ENST00000706713.1:c.547G>T	ENSP00000516510.1:p.Glu183Ter
ENST00000706714.1:c.533G>T	ENSP00000516511.1:p.Gly178Val
ENST00000706715.1:c.169G>T	ENSP00000516512.1:p.Glu57Ter
ENST00000354171.13:c.553G>T MANE Select	ENSP00000346103.7:p.Glu185Ter
ENST00000589115.6:c.528G>T	ENSP00000466872.3:p.Arg176Ser
ENST00000354171.12:c.553G>T	ENSP00000346103.7:p.Glu185Ter
ENST00000585480.1:c.286G>T	ENSP00000467900.1:p.Glu96Ter
ENST00000587648.5:c.433G>T	ENSP00000468349.1:p.Glu145Ter
ENST00000588919.5:c.494G>T	ENSP00000464989.3:p.Gly165Val
ENST00000589115.5:c.528G>T	ENSP00000466872.2:p.Arg176Ser
ENST00000592940.2:n.924G>T
ENST00000611653.4:c.472G>T	ENSP00000483655.1:p.Glu158Ter
ENST00000616066.4:c.550G>T	ENSP00000485000.1:p.Glu184Ter
ENST00000622390.4:c.661G>T	ENSP00000477503.1:p.Glu221Ter
NM_001039847.2:c.575G>T	NP_001034936.1:p.Gly192Val
NM_001039848.2:c.664G>T	NP_001034937.1:p.Glu222Ter
NM_002085.4:c.553G>T	NP_002076.2:p.Glu185Ter
NM_001039848.3:c.664G>T	NP_001034937.1:p.Glu222Ter
NM_001039847.3:c.575G>T	NP_001034936.1:p.Gly192Val
NM_001039848.4:c.664G>T	NP_001034937.1:p.Glu222Ter
NM_001367832.1:c.472G>T	NP_001354761.1:p.Glu158Ter
NM_002085.5:c.553G>T MANE Select	NP_002076.2:p.Glu185Ter