Canonical Allele Identifier: CA658658763

Gene: GPX4

Linked Data

• ClinVar Variation Id: 451510
• ClinVar RCV Id: RCV000521481 ; RCV001844185
• dbSNP Id: rs1555716575
• MyVariant Identifiers: chr19:g.1106398del (hg19) ; chr19:g.1106399del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106399del , CM000681.2:g.1106399del	GRCh38
NC_000019.9:g.1106398del , CM000681.1:g.1106398del	GRCh37
NC_000019.8:g.1057398del	NCBI36
NG_050621.1:g.7474del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.613-1del	ENSP00000473614.3:n.613-1del
ENST00000593032.6:c.482-1del	ENSP00000465828.4:n.482-1del
ENST00000706713.1:c.496-1del	ENSP00000516510.1:n.496-1del
ENST00000706714.1:c.482-1del	ENSP00000516511.1:n.482-1del
ENST00000706715.1:c.118-1del	ENSP00000516512.1:n.118-1del
ENST00000354171.13:c.502-1del MANE Select	ENSP00000346103.7:n.502-1del
ENST00000589115.6:c.477-1del	ENSP00000466872.3:n.477-1del
ENST00000354171.12:c.502-1del	ENSP00000346103.7:n.502-1del
ENST00000585480.1:c.235-1del	ENSP00000467900.1:n.235-1del
ENST00000587648.5:c.382-1del	ENSP00000468349.1:n.382-1del
ENST00000588919.5:c.442del	ENSP00000464989.3:p.Val148PhefsTer?
ENST00000589115.5:c.477-1del	ENSP00000466872.2:n.477-1del
ENST00000592940.2:n.873-1del
ENST00000593032.5:c.482-1del	ENSP00000465828.3:n.482-1del
ENST00000611653.4:c.421-1del	ENSP00000483655.1:n.421-1del
ENST00000616066.4:c.499-1del	ENSP00000485000.1:n.499-1del
ENST00000622390.4:c.610-1del	ENSP00000477503.1:n.610-1del
NM_001039847.2:c.523del	NP_001034936.1:p.Val175PhefsTer?
NM_001039848.2:c.613-1del	NP_001034937.1:n.613-1del
NM_002085.4:c.502-1del	NP_002076.2:n.502-1del
NM_001039848.3:c.613-1del	NP_001034937.1:n.613-1del
NM_001039847.3:c.523del	NP_001034936.1:p.Val175PhefsTer?
NM_001039848.4:c.613-1del	NP_001034937.1:n.613-1del
NM_001367832.1:c.421-1del	NP_001354761.1:n.421-1del
NM_002085.5:c.502-1del MANE Select	NP_002076.2:n.502-1del