Canonical Allele Identifier: CA402940146

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106451A>T (hg19) ; chr19:g.1106452A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106452A>T , CM000681.2:g.1106452A>T	GRCh38
NC_000019.9:g.1106451A>T , CM000681.1:g.1106451A>T	GRCh37
NC_000019.8:g.1057451A>T	NCBI36
NG_050621.1:g.7527A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.665A>T	ENSP00000473614.3:p.Glu222Val
ENST00000593032.6:c.534A>T	ENSP00000465828.4:p.Gly178=
ENST00000706713.1:c.548A>T	ENSP00000516510.1:p.Glu183Val
ENST00000706714.1:c.534A>T	ENSP00000516511.1:p.Gly178=
ENST00000706715.1:c.170A>T	ENSP00000516512.1:p.Glu57Val
ENST00000354171.13:c.554A>T MANE Select	ENSP00000346103.7:p.Glu185Val
ENST00000589115.6:c.529A>T	ENSP00000466872.3:p.Ser177Cys
ENST00000354171.12:c.554A>T	ENSP00000346103.7:p.Glu185Val
ENST00000585480.1:c.287A>T	ENSP00000467900.1:p.Glu96Val
ENST00000587648.5:c.434A>T	ENSP00000468349.1:p.Glu145Val
ENST00000588919.5:c.495A>T	ENSP00000464989.3:p.Gly165=
ENST00000589115.5:c.529A>T	ENSP00000466872.2:p.Ser177Cys
ENST00000592940.2:n.925A>T
ENST00000611653.4:c.473A>T	ENSP00000483655.1:p.Glu158Val
ENST00000616066.4:c.551A>T	ENSP00000485000.1:p.Glu184Val
ENST00000622390.4:c.662A>T	ENSP00000477503.1:p.Glu221Val
NM_001039847.2:c.576A>T	NP_001034936.1:p.Gly192=
NM_001039848.2:c.665A>T	NP_001034937.1:p.Glu222Val
NM_002085.4:c.554A>T	NP_002076.2:p.Glu185Val
NM_001039848.3:c.665A>T	NP_001034937.1:p.Glu222Val
NM_001039847.3:c.576A>T	NP_001034936.1:p.Gly192=
NM_001039848.4:c.665A>T	NP_001034937.1:p.Glu222Val
NM_001367832.1:c.473A>T	NP_001354761.1:p.Glu158Val
NM_002085.5:c.554A>T MANE Select	NP_002076.2:p.Glu185Val