Canonical Allele Identifier: CA402937556

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105736T>C (hg19) ; chr19:g.1105737T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105737T>C , CM000681.2:g.1105737T>C	GRCh38
NC_000019.9:g.1105736T>C , CM000681.1:g.1105736T>C	GRCh37
NC_000019.8:g.1056736T>C	NCBI36
NG_050621.1:g.6812T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.515T>C	ENSP00000473614.3:p.Val172Ala
ENST00000593032.6:c.323T>C	ENSP00000465828.4:p.Val108Ala
ENST00000706713.1:c.398T>C	ENSP00000516510.1:p.Val133Ala
ENST00000706714.1:c.323T>C	ENSP00000516511.1:p.Val108Ala
ENST00000706715.1:c.20T>C	ENSP00000516512.1:p.Val7Ala
ENST00000354171.13:c.404T>C MANE Select	ENSP00000346103.7:p.Val135Ala
ENST00000589115.6:c.404T>C	ENSP00000466872.3:p.Val135Ala
ENST00000354171.12:c.404T>C	ENSP00000346103.7:p.Val135Ala
ENST00000585362.6:c.515T>C	ENSP00000473614.2:p.Val172Ala
ENST00000585480.1:c.137T>C	ENSP00000467900.1:p.Val46Ala
ENST00000587648.5:c.284T>C	ENSP00000468349.1:p.Val95Ala
ENST00000588919.5:c.323T>C	ENSP00000464989.3:p.Val108Ala
ENST00000589115.5:c.404T>C	ENSP00000466872.2:p.Val135Ala
ENST00000592940.2:n.343T>C
ENST00000593032.5:c.323T>C	ENSP00000465828.3:p.Val108Ala
ENST00000611653.4:c.323T>C	ENSP00000483655.1:p.Val108Ala
ENST00000616066.4:c.401T>C	ENSP00000485000.1:p.Val134Ala
ENST00000622390.4:c.512T>C	ENSP00000477503.1:p.Val171Ala
NM_001039847.2:c.404T>C	NP_001034936.1:p.Val135Ala
NM_001039848.2:c.515T>C	NP_001034937.1:p.Val172Ala
NM_002085.4:c.404T>C	NP_002076.2:p.Val135Ala
NM_001039848.3:c.515T>C	NP_001034937.1:p.Val172Ala
NM_001039847.3:c.404T>C	NP_001034936.1:p.Val135Ala
NM_001039848.4:c.515T>C	NP_001034937.1:p.Val172Ala
NM_001367832.1:c.323T>C	NP_001354761.1:p.Val108Ala
NM_002085.5:c.404T>C MANE Select	NP_002076.2:p.Val135Ala