Canonical Allele Identifier: CA402939701

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106407-T-C
• MyVariant Identifiers: chr19:g.1106406T>C (hg19) ; chr19:g.1106407T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.620T>C	ENSP00000473614.3:p.Ile207Thr
ENST00000593032.6:c.489T>C	ENSP00000465828.4:p.His163=
ENST00000706713.1:c.503T>C	ENSP00000516510.1:p.Ile168Thr
ENST00000706714.1:c.489T>C	ENSP00000516511.1:p.His163=
ENST00000706715.1:c.125T>C	ENSP00000516512.1:p.Ile42Thr
ENST00000354171.13:c.509T>C MANE Select	ENSP00000346103.7:p.Ile170Thr
ENST00000589115.6:c.484T>C	ENSP00000466872.3:p.Ser162Pro
ENST00000354171.12:c.509T>C	ENSP00000346103.7:p.Ile170Thr
ENST00000585480.1:c.242T>C	ENSP00000467900.1:p.Ile81Thr
ENST00000587648.5:c.389T>C	ENSP00000468349.1:p.Ile130Thr
ENST00000588919.5:c.450T>C	ENSP00000464989.3:p.His150=
ENST00000589115.5:c.484T>C	ENSP00000466872.2:p.Ser162Pro
ENST00000592940.2:n.880T>C
ENST00000593032.5:c.489T>C	ENSP00000465828.3:p.His163=
ENST00000611653.4:c.428T>C	ENSP00000483655.1:p.Ile143Thr
ENST00000616066.4:c.506T>C	ENSP00000485000.1:p.Ile169Thr
ENST00000622390.4:c.617T>C	ENSP00000477503.1:p.Ile206Thr
NM_001039847.2:c.531T>C	NP_001034936.1:p.His177=
NM_001039848.2:c.620T>C	NP_001034937.1:p.Ile207Thr
NM_002085.4:c.509T>C	NP_002076.2:p.Ile170Thr
NM_001039848.3:c.620T>C	NP_001034937.1:p.Ile207Thr
NM_001039847.3:c.531T>C	NP_001034936.1:p.His177=
NM_001039848.4:c.620T>C	NP_001034937.1:p.Ile207Thr
NM_001367832.1:c.428T>C	NP_001354761.1:p.Ile143Thr
NM_002085.5:c.509T>C MANE Select	NP_002076.2:p.Ile170Thr