Canonical Allele Identifier: CA402940055

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106438G>C (hg19) ; chr19:g.1106439G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106439G>C , CM000681.2:g.1106439G>C	GRCh38
NC_000019.9:g.1106438G>C , CM000681.1:g.1106438G>C	GRCh37
NC_000019.8:g.1057438G>C	NCBI36
NG_050621.1:g.7514G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.652G>C	ENSP00000473614.3:p.Gly218Arg
ENST00000593032.6:c.521G>C	ENSP00000465828.4:p.Arg174Pro
ENST00000706713.1:c.535G>C	ENSP00000516510.1:p.Gly179Arg
ENST00000706714.1:c.521G>C	ENSP00000516511.1:p.Arg174Pro
ENST00000706715.1:c.157G>C	ENSP00000516512.1:p.Gly53Arg
ENST00000354171.13:c.541G>C MANE Select	ENSP00000346103.7:p.Gly181Arg
ENST00000589115.6:c.516G>C	ENSP00000466872.3:p.Thr172=
ENST00000354171.12:c.541G>C	ENSP00000346103.7:p.Gly181Arg
ENST00000585480.1:c.274G>C	ENSP00000467900.1:p.Gly92Arg
ENST00000587648.5:c.421G>C	ENSP00000468349.1:p.Gly141Arg
ENST00000588919.5:c.482G>C	ENSP00000464989.3:p.Arg161Pro
ENST00000589115.5:c.516G>C	ENSP00000466872.2:p.Thr172=
ENST00000592940.2:n.912G>C
ENST00000593032.5:c.521G>C	ENSP00000465828.3:p.Arg174Pro
ENST00000611653.4:c.460G>C	ENSP00000483655.1:p.Gly154Arg
ENST00000616066.4:c.538G>C	ENSP00000485000.1:p.Gly180Arg
ENST00000622390.4:c.649G>C	ENSP00000477503.1:p.Gly217Arg
NM_001039847.2:c.563G>C	NP_001034936.1:p.Arg188Pro
NM_001039848.2:c.652G>C	NP_001034937.1:p.Gly218Arg
NM_002085.4:c.541G>C	NP_002076.2:p.Gly181Arg
NM_001039848.3:c.652G>C	NP_001034937.1:p.Gly218Arg
NM_001039847.3:c.563G>C	NP_001034936.1:p.Arg188Pro
NM_001039848.4:c.652G>C	NP_001034937.1:p.Gly218Arg
NM_001367832.1:c.460G>C	NP_001354761.1:p.Gly154Arg
NM_002085.5:c.541G>C MANE Select	NP_002076.2:p.Gly181Arg