Canonical Allele Identifier: CA402940114

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106448A>T (hg19) ; chr19:g.1106449A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106449A>T , CM000681.2:g.1106449A>T	GRCh38
NC_000019.9:g.1106448A>T , CM000681.1:g.1106448A>T	GRCh37
NC_000019.8:g.1057448A>T	NCBI36
NG_050621.1:g.7524A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.662A>T	ENSP00000473614.3:p.Glu221Val
ENST00000593032.6:c.531A>T	ENSP00000465828.4:p.Gly177=
ENST00000706713.1:c.545A>T	ENSP00000516510.1:p.Glu182Val
ENST00000706714.1:c.531A>T	ENSP00000516511.1:p.Gly177=
ENST00000706715.1:c.167A>T	ENSP00000516512.1:p.Glu56Val
ENST00000354171.13:c.551A>T MANE Select	ENSP00000346103.7:p.Glu184Val
ENST00000589115.6:c.526A>T	ENSP00000466872.3:p.Arg176Trp
ENST00000354171.12:c.551A>T	ENSP00000346103.7:p.Glu184Val
ENST00000585480.1:c.284A>T	ENSP00000467900.1:p.Glu95Val
ENST00000587648.5:c.431A>T	ENSP00000468349.1:p.Glu144Val
ENST00000588919.5:c.492A>T	ENSP00000464989.3:p.Gly164=
ENST00000589115.5:c.526A>T	ENSP00000466872.2:p.Arg176Trp
ENST00000592940.2:n.922A>T
ENST00000611653.4:c.470A>T	ENSP00000483655.1:p.Glu157Val
ENST00000616066.4:c.548A>T	ENSP00000485000.1:p.Glu183Val
ENST00000622390.4:c.659A>T	ENSP00000477503.1:p.Glu220Val
NM_001039847.2:c.573A>T	NP_001034936.1:p.Gly191=
NM_001039848.2:c.662A>T	NP_001034937.1:p.Glu221Val
NM_002085.4:c.551A>T	NP_002076.2:p.Glu184Val
NM_001039848.3:c.662A>T	NP_001034937.1:p.Glu221Val
NM_001039847.3:c.573A>T	NP_001034936.1:p.Gly191=
NM_001039848.4:c.662A>T	NP_001034937.1:p.Glu221Val
NM_001367832.1:c.470A>T	NP_001354761.1:p.Glu157Val
NM_002085.5:c.551A>T MANE Select	NP_002076.2:p.Glu184Val