Canonical Allele Identifier: CA402939853

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106418G>T (hg19) ; chr19:g.1106419G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106419G>T , CM000681.2:g.1106419G>T	GRCh38
NC_000019.9:g.1106418G>T , CM000681.1:g.1106418G>T	GRCh37
NC_000019.8:g.1057418G>T	NCBI36
NG_050621.1:g.7494G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.632G>T	ENSP00000473614.3:p.Gly211Val
ENST00000593032.6:c.501G>T	ENSP00000465828.4:p.Arg167=
ENST00000706713.1:c.515G>T	ENSP00000516510.1:p.Gly172Val
ENST00000706714.1:c.501G>T	ENSP00000516511.1:p.Arg167=
ENST00000706715.1:c.137G>T	ENSP00000516512.1:p.Gly46Val
ENST00000354171.13:c.521G>T MANE Select	ENSP00000346103.7:p.Gly174Val
ENST00000589115.6:c.496G>T	ENSP00000466872.3:p.Ala166Ser
ENST00000354171.12:c.521G>T	ENSP00000346103.7:p.Gly174Val
ENST00000585480.1:c.254G>T	ENSP00000467900.1:p.Gly85Val
ENST00000587648.5:c.401G>T	ENSP00000468349.1:p.Gly134Val
ENST00000588919.5:c.462G>T	ENSP00000464989.3:p.Arg154=
ENST00000589115.5:c.496G>T	ENSP00000466872.2:p.Ala166Ser
ENST00000592940.2:n.892G>T
ENST00000593032.5:c.501G>T	ENSP00000465828.3:p.Arg167=
ENST00000611653.4:c.440G>T	ENSP00000483655.1:p.Gly147Val
ENST00000616066.4:c.518G>T	ENSP00000485000.1:p.Gly173Val
ENST00000622390.4:c.629G>T	ENSP00000477503.1:p.Gly210Val
NM_001039847.2:c.543G>T	NP_001034936.1:p.Arg181=
NM_001039848.2:c.632G>T	NP_001034937.1:p.Gly211Val
NM_002085.4:c.521G>T	NP_002076.2:p.Gly174Val
NM_001039848.3:c.632G>T	NP_001034937.1:p.Gly211Val
NM_001039847.3:c.543G>T	NP_001034936.1:p.Arg181=
NM_001039848.4:c.632G>T	NP_001034937.1:p.Gly211Val
NM_001367832.1:c.440G>T	NP_001354761.1:p.Gly147Val
NM_002085.5:c.521G>T MANE Select	NP_002076.2:p.Gly174Val