Canonical Allele Identifier: CA402937609

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105763G>C (hg19) ; chr19:g.1105764G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105764G>C , CM000681.2:g.1105764G>C	GRCh38
NC_000019.9:g.1105763G>C , CM000681.1:g.1105763G>C	GRCh37
NC_000019.8:g.1056763G>C	NCBI36
NG_050621.1:g.6839G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.542G>C	ENSP00000473614.3:p.Trp181Ser
ENST00000593032.6:c.350G>C	ENSP00000465828.4:p.Trp117Ser
ENST00000706713.1:c.425G>C	ENSP00000516510.1:p.Trp142Ser
ENST00000706714.1:c.350G>C	ENSP00000516511.1:p.Trp117Ser
ENST00000706715.1:c.47G>C	ENSP00000516512.1:p.Trp16Ser
ENST00000354171.13:c.431G>C MANE Select	ENSP00000346103.7:p.Trp144Ser
ENST00000589115.6:c.431G>C	ENSP00000466872.3:p.Trp144Ser
ENST00000354171.12:c.431G>C	ENSP00000346103.7:p.Trp144Ser
ENST00000585480.1:c.164G>C	ENSP00000467900.1:p.Trp55Ser
ENST00000587648.5:c.311G>C	ENSP00000468349.1:p.Trp104Ser
ENST00000588919.5:c.350G>C	ENSP00000464989.3:p.Trp117Ser
ENST00000589115.5:c.431G>C	ENSP00000466872.2:p.Trp144Ser
ENST00000592940.2:n.370G>C
ENST00000593032.5:c.350G>C	ENSP00000465828.3:p.Trp117Ser
ENST00000611653.4:c.350G>C	ENSP00000483655.1:p.Trp117Ser
ENST00000616066.4:c.428G>C	ENSP00000485000.1:p.Trp143Ser
ENST00000622390.4:c.539G>C	ENSP00000477503.1:p.Trp180Ser
NM_001039847.2:c.431G>C	NP_001034936.1:p.Trp144Ser
NM_001039848.2:c.542G>C	NP_001034937.1:p.Trp181Ser
NM_002085.4:c.431G>C	NP_002076.2:p.Trp144Ser
NM_001039848.3:c.542G>C	NP_001034937.1:p.Trp181Ser
NM_001039847.3:c.431G>C	NP_001034936.1:p.Trp144Ser
NM_001039848.4:c.542G>C	NP_001034937.1:p.Trp181Ser
NM_001367832.1:c.350G>C	NP_001354761.1:p.Trp117Ser
NM_002085.5:c.431G>C MANE Select	NP_002076.2:p.Trp144Ser