Canonical Allele Identifier: CA402940067

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106439G>T (hg19) ; chr19:g.1106440G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106440G>T , CM000681.2:g.1106440G>T	GRCh38
NC_000019.9:g.1106439G>T , CM000681.1:g.1106439G>T	GRCh37
NC_000019.8:g.1057439G>T	NCBI36
NG_050621.1:g.7515G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.653G>T	ENSP00000473614.3:p.Gly218Val
ENST00000593032.6:c.522G>T	ENSP00000465828.4:p.Arg174=
ENST00000706713.1:c.536G>T	ENSP00000516510.1:p.Gly179Val
ENST00000706714.1:c.522G>T	ENSP00000516511.1:p.Arg174=
ENST00000706715.1:c.158G>T	ENSP00000516512.1:p.Gly53Val
ENST00000354171.13:c.542G>T MANE Select	ENSP00000346103.7:p.Gly181Val
ENST00000589115.6:c.517G>T	ENSP00000466872.3:p.Asp173Tyr
ENST00000354171.12:c.542G>T	ENSP00000346103.7:p.Gly181Val
ENST00000585480.1:c.275G>T	ENSP00000467900.1:p.Gly92Val
ENST00000587648.5:c.422G>T	ENSP00000468349.1:p.Gly141Val
ENST00000588919.5:c.483G>T	ENSP00000464989.3:p.Arg161=
ENST00000589115.5:c.517G>T	ENSP00000466872.2:p.Asp173Tyr
ENST00000592940.2:n.913G>T
ENST00000593032.5:c.522G>T	ENSP00000465828.3:p.Arg174=
ENST00000611653.4:c.461G>T	ENSP00000483655.1:p.Gly154Val
ENST00000616066.4:c.539G>T	ENSP00000485000.1:p.Gly180Val
ENST00000622390.4:c.650G>T	ENSP00000477503.1:p.Gly217Val
NM_001039847.2:c.564G>T	NP_001034936.1:p.Arg188=
NM_001039848.2:c.653G>T	NP_001034937.1:p.Gly218Val
NM_002085.4:c.542G>T	NP_002076.2:p.Gly181Val
NM_001039848.3:c.653G>T	NP_001034937.1:p.Gly218Val
NM_001039847.3:c.564G>T	NP_001034936.1:p.Arg188=
NM_001039848.4:c.653G>T	NP_001034937.1:p.Gly218Val
NM_001367832.1:c.461G>T	NP_001354761.1:p.Gly154Val
NM_002085.5:c.542G>T MANE Select	NP_002076.2:p.Gly181Val