Canonical Allele Identifier: CA402939697

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106406T>A (hg19) ; chr19:g.1106407T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106407T>A , CM000681.2:g.1106407T>A	GRCh38
NC_000019.9:g.1106406T>A , CM000681.1:g.1106406T>A	GRCh37
NC_000019.8:g.1057406T>A	NCBI36
NG_050621.1:g.7482T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.620T>A	ENSP00000473614.3:p.Ile207Asn
ENST00000593032.6:c.489T>A	ENSP00000465828.4:p.His163Gln
ENST00000706713.1:c.503T>A	ENSP00000516510.1:p.Ile168Asn
ENST00000706714.1:c.489T>A	ENSP00000516511.1:p.His163Gln
ENST00000706715.1:c.125T>A	ENSP00000516512.1:p.Ile42Asn
ENST00000354171.13:c.509T>A MANE Select	ENSP00000346103.7:p.Ile170Asn
ENST00000589115.6:c.484T>A	ENSP00000466872.3:p.Ser162Thr
ENST00000354171.12:c.509T>A	ENSP00000346103.7:p.Ile170Asn
ENST00000585480.1:c.242T>A	ENSP00000467900.1:p.Ile81Asn
ENST00000587648.5:c.389T>A	ENSP00000468349.1:p.Ile130Asn
ENST00000588919.5:c.450T>A	ENSP00000464989.3:p.His150Gln
ENST00000589115.5:c.484T>A	ENSP00000466872.2:p.Ser162Thr
ENST00000592940.2:n.880T>A
ENST00000593032.5:c.489T>A	ENSP00000465828.3:p.His163Gln
ENST00000611653.4:c.428T>A	ENSP00000483655.1:p.Ile143Asn
ENST00000616066.4:c.506T>A	ENSP00000485000.1:p.Ile169Asn
ENST00000622390.4:c.617T>A	ENSP00000477503.1:p.Ile206Asn
NM_001039847.2:c.531T>A	NP_001034936.1:p.His177Gln
NM_001039848.2:c.620T>A	NP_001034937.1:p.Ile207Asn
NM_002085.4:c.509T>A	NP_002076.2:p.Ile170Asn
NM_001039848.3:c.620T>A	NP_001034937.1:p.Ile207Asn
NM_001039847.3:c.531T>A	NP_001034936.1:p.His177Gln
NM_001039848.4:c.620T>A	NP_001034937.1:p.Ile207Asn
NM_001367832.1:c.428T>A	NP_001354761.1:p.Ile143Asn
NM_002085.5:c.509T>A MANE Select	NP_002076.2:p.Ile170Asn