Canonical Allele Identifier: CA402940154

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106452G>T (hg19) ; chr19:g.1106453G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106453G>T , CM000681.2:g.1106453G>T	GRCh38
NC_000019.9:g.1106452G>T , CM000681.1:g.1106452G>T	GRCh37
NC_000019.8:g.1057452G>T	NCBI36
NG_050621.1:g.7528G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.666G>T	ENSP00000473614.3:p.Glu222Asp
ENST00000593032.6:c.535G>T	ENSP00000465828.4:p.Ala179Ser
ENST00000706713.1:c.549G>T	ENSP00000516510.1:p.Glu183Asp
ENST00000706714.1:c.535G>T	ENSP00000516511.1:p.Ala179Ser
ENST00000706715.1:c.171G>T	ENSP00000516512.1:p.Glu57Asp
ENST00000354171.13:c.555G>T MANE Select	ENSP00000346103.7:p.Glu185Asp
ENST00000589115.6:c.530G>T	ENSP00000466872.3:p.Ser177Ile
ENST00000354171.12:c.555G>T	ENSP00000346103.7:p.Glu185Asp
ENST00000585480.1:c.288G>T	ENSP00000467900.1:p.Glu96Asp
ENST00000587648.5:c.435G>T	ENSP00000468349.1:p.Glu145Asp
ENST00000588919.5:c.496G>T	ENSP00000464989.3:p.Ala166Ser
ENST00000589115.5:c.530G>T	ENSP00000466872.2:p.Ser177Ile
ENST00000592940.2:n.926G>T
ENST00000611653.4:c.474G>T	ENSP00000483655.1:p.Glu158Asp
ENST00000616066.4:c.552G>T	ENSP00000485000.1:p.Glu184Asp
ENST00000622390.4:c.663G>T	ENSP00000477503.1:p.Glu221Asp
NM_001039847.2:c.577G>T	NP_001034936.1:p.Ala193Ser
NM_001039848.2:c.666G>T	NP_001034937.1:p.Glu222Asp
NM_002085.4:c.555G>T	NP_002076.2:p.Glu185Asp
NM_001039848.3:c.666G>T	NP_001034937.1:p.Glu222Asp
NM_001039847.3:c.577G>T	NP_001034936.1:p.Ala193Ser
NM_001039848.4:c.666G>T	NP_001034937.1:p.Glu222Asp
NM_001367832.1:c.474G>T	NP_001354761.1:p.Glu158Asp
NM_002085.5:c.555G>T MANE Select	NP_002076.2:p.Glu185Asp