Canonical Allele Identifier: CA163453

Gene: GPX4

Linked Data

• ClinVar Variation Id: 140617
• ClinVar RCV Id: RCV000128833
• dbSNP Id: rs769967246
• MyVariant Identifiers: chr19:g.1105455C>A (hg19) ; chr19:g.1105456C>A (hg38)
• PubMed: PMID:22529034 ; PMID:24706940

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105456C>A , CM000681.2:g.1105456C>A	GRCh38
NC_000019.9:g.1105455C>A , CM000681.1:g.1105455C>A	GRCh37
NC_000019.8:g.1056455C>A	NCBI36
NG_050621.1:g.6531C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.381C>A	ENSP00000473614.3:p.Tyr127Ter
ENST00000593032.6:c.189C>A	ENSP00000465828.4:p.Tyr63Ter
ENST00000706713.1:c.264C>A	ENSP00000516510.1:p.Tyr88Ter
ENST00000706714.1:c.189C>A	ENSP00000516511.1:p.Tyr63Ter
ENST00000706715.1:c.-115C>A	ENSP00000516512.1:n.-115C>A
ENST00000354171.13:c.270C>A MANE Select	ENSP00000346103.7:p.Tyr90Ter
ENST00000589115.6:c.270C>A	ENSP00000466872.3:p.Tyr90Ter
ENST00000354171.12:c.270C>A	ENSP00000346103.7:p.Tyr90Ter
ENST00000585362.6:c.381C>A	ENSP00000473614.2:p.Tyr127Ter
ENST00000585480.1:c.3C>A	ENSP00000467900.1:p.Tyr1Ter
ENST00000587648.5:c.150C>A	ENSP00000468349.1:p.Tyr50Ter
ENST00000587932.2:n.204C>A
ENST00000588919.5:c.189C>A	ENSP00000464989.3:p.Tyr63Ter
ENST00000589115.5:c.270C>A	ENSP00000466872.2:p.Tyr90Ter
ENST00000592940.2:n.216C>A
ENST00000593032.5:c.189C>A	ENSP00000465828.3:p.Tyr63Ter
ENST00000611653.4:c.189C>A	ENSP00000483655.1:p.Tyr63Ter
ENST00000614791.1:c.375C>A	ENSP00000484697.1:p.Tyr125Ter
ENST00000616066.4:c.267C>A	ENSP00000485000.1:p.Tyr89Ter
ENST00000622390.4:c.378C>A	ENSP00000477503.1:p.Tyr126Ter
NM_001039847.2:c.270C>A	NP_001034936.1:p.Tyr90Ter
NM_001039848.2:c.381C>A	NP_001034937.1:p.Tyr127Ter
NM_002085.4:c.270C>A	NP_002076.2:p.Tyr90Ter
NM_001039848.3:c.381C>A	NP_001034937.1:p.Tyr127Ter
NM_001039847.3:c.270C>A	NP_001034936.1:p.Tyr90Ter
NM_001039848.4:c.381C>A	NP_001034937.1:p.Tyr127Ter
NM_001367832.1:c.189C>A	NP_001354761.1:p.Tyr63Ter
NM_002085.5:c.270C>A MANE Select	NP_002076.2:p.Tyr90Ter