Canonical Allele Identifier: CA402940133

Gene: GPX4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.664G>C	ENSP00000473614.3:p.Glu222Gln
ENST00000593032.6:c.533G>C	ENSP00000465828.4:p.Gly178Ala
ENST00000706713.1:c.547G>C	ENSP00000516510.1:p.Glu183Gln
ENST00000706714.1:c.533G>C	ENSP00000516511.1:p.Gly178Ala
ENST00000706715.1:c.169G>C	ENSP00000516512.1:p.Glu57Gln
ENST00000354171.13:c.553G>C MANE Select	ENSP00000346103.7:p.Glu185Gln
ENST00000589115.6:c.528G>C	ENSP00000466872.3:p.Arg176Ser
ENST00000354171.12:c.553G>C	ENSP00000346103.7:p.Glu185Gln
ENST00000585480.1:c.286G>C	ENSP00000467900.1:p.Glu96Gln
ENST00000587648.5:c.433G>C	ENSP00000468349.1:p.Glu145Gln
ENST00000588919.5:c.494G>C	ENSP00000464989.3:p.Gly165Ala
ENST00000589115.5:c.528G>C	ENSP00000466872.2:p.Arg176Ser
ENST00000592940.2:n.924G>C
ENST00000611653.4:c.472G>C	ENSP00000483655.1:p.Glu158Gln
ENST00000616066.4:c.550G>C	ENSP00000485000.1:p.Glu184Gln
ENST00000622390.4:c.661G>C	ENSP00000477503.1:p.Glu221Gln
NM_001039847.2:c.575G>C	NP_001034936.1:p.Gly192Ala
NM_001039848.2:c.664G>C	NP_001034937.1:p.Glu222Gln
NM_002085.4:c.553G>C	NP_002076.2:p.Glu185Gln
NM_001039848.3:c.664G>C	NP_001034937.1:p.Glu222Gln
NM_001039847.3:c.575G>C	NP_001034936.1:p.Gly192Ala
NM_001039848.4:c.664G>C	NP_001034937.1:p.Glu222Gln
NM_001367832.1:c.472G>C	NP_001354761.1:p.Glu158Gln
NM_002085.5:c.553G>C MANE Select	NP_002076.2:p.Glu185Gln