Canonical Allele Identifier: CA402940181

Gene: GPX4

Linked Data

• dbSNP Id: rs2079658330
• gnomAD v4: 19-1106458-T-C
• MyVariant Identifiers: chr19:g.1106457T>C (hg19) ; chr19:g.1106458T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106458T>C , CM000681.2:g.1106458T>C	GRCh38
NC_000019.9:g.1106457T>C , CM000681.1:g.1106457T>C	GRCh37
NC_000019.8:g.1057457T>C	NCBI36
NG_050621.1:g.7533T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.671T>C	ENSP00000473614.3:p.Leu224Pro
ENST00000593032.6:c.540T>C	ENSP00000465828.4:p.Pro180=
ENST00000706713.1:c.554T>C	ENSP00000516510.1:p.Leu185Pro
ENST00000706714.1:c.540T>C	ENSP00000516511.1:p.Pro180=
ENST00000706715.1:c.176T>C	ENSP00000516512.1:p.Leu59Pro
ENST00000354171.13:c.560T>C MANE Select	ENSP00000346103.7:p.Leu187Pro
ENST00000589115.6:c.535T>C	ENSP00000466872.3:p.Trp179Arg
ENST00000354171.12:c.560T>C	ENSP00000346103.7:p.Leu187Pro
ENST00000585480.1:c.293T>C	ENSP00000467900.1:p.Leu98Pro
ENST00000587648.5:c.440T>C	ENSP00000468349.1:p.Leu147Pro
ENST00000588919.5:c.501T>C	ENSP00000464989.3:p.Pro167=
ENST00000589115.5:c.535T>C	ENSP00000466872.2:p.Trp179Arg
ENST00000592940.2:n.931T>C
ENST00000611653.4:c.479T>C	ENSP00000483655.1:p.Leu160Pro
ENST00000616066.4:c.557T>C	ENSP00000485000.1:p.Leu186Pro
ENST00000622390.4:c.668T>C	ENSP00000477503.1:p.Leu223Pro
NM_001039847.2:c.582T>C	NP_001034936.1:p.Pro194=
NM_001039848.2:c.671T>C	NP_001034937.1:p.Leu224Pro
NM_002085.4:c.560T>C	NP_002076.2:p.Leu187Pro
NM_001039848.3:c.671T>C	NP_001034937.1:p.Leu224Pro
NM_001039847.3:c.582T>C	NP_001034936.1:p.Pro194=
NM_001039848.4:c.671T>C	NP_001034937.1:p.Leu224Pro
NM_001367832.1:c.479T>C	NP_001354761.1:p.Leu160Pro
NM_002085.5:c.560T>C MANE Select	NP_002076.2:p.Leu187Pro