Canonical Allele Identifier: CA402940017

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106434C>T (hg19) ; chr19:g.1106435C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106435C>T , CM000681.2:g.1106435C>T	GRCh38
NC_000019.9:g.1106434C>T , CM000681.1:g.1106434C>T	GRCh37
NC_000019.8:g.1057434C>T	NCBI36
NG_050621.1:g.7510C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.648C>T	ENSP00000473614.3:p.Arg216=
ENST00000593032.6:c.517C>T	ENSP00000465828.4:p.Leu173=
ENST00000706713.1:c.531C>T	ENSP00000516510.1:p.Arg177=
ENST00000706714.1:c.517C>T	ENSP00000516511.1:p.Leu173=
ENST00000706715.1:c.153C>T	ENSP00000516512.1:p.Arg51=
ENST00000354171.13:c.537C>T MANE Select	ENSP00000346103.7:p.Arg179=
ENST00000589115.6:c.512C>T	ENSP00000466872.3:p.Ala171Val
ENST00000354171.12:c.537C>T	ENSP00000346103.7:p.Arg179=
ENST00000585480.1:c.270C>T	ENSP00000467900.1:p.Arg90=
ENST00000587648.5:c.417C>T	ENSP00000468349.1:p.Arg139=
ENST00000588919.5:c.478C>T	ENSP00000464989.3:p.Leu160=
ENST00000589115.5:c.512C>T	ENSP00000466872.2:p.Ala171Val
ENST00000592940.2:n.908C>T
ENST00000593032.5:c.517C>T	ENSP00000465828.3:p.Leu173=
ENST00000611653.4:c.456C>T	ENSP00000483655.1:p.Arg152=
ENST00000616066.4:c.534C>T	ENSP00000485000.1:p.Arg178=
ENST00000622390.4:c.645C>T	ENSP00000477503.1:p.Arg215=
NM_001039847.2:c.559C>T	NP_001034936.1:p.Leu187=
NM_001039848.2:c.648C>T	NP_001034937.1:p.Arg216=
NM_002085.4:c.537C>T	NP_002076.2:p.Arg179=
NM_001039848.3:c.648C>T	NP_001034937.1:p.Arg216=
NM_001039847.3:c.559C>T	NP_001034936.1:p.Leu187=
NM_001039848.4:c.648C>T	NP_001034937.1:p.Arg216=
NM_001367832.1:c.456C>T	NP_001354761.1:p.Arg152=
NM_002085.5:c.537C>T MANE Select	NP_002076.2:p.Arg179=