Canonical Allele Identifier: CA9037467

Gene: GPX4

Linked Data

• ClinVar Variation Id: 1514972
• ClinVar RCV Id: RCV002029696
• dbSNP Id: rs768879858
• ExAC: 19:1106409 A / G
• gnomAD v2: 19-1106409-A-G
• gnomAD v3: 19-1106410-A-G
• gnomAD v4: 19-1106410-A-G
• MyVariant Identifiers: chr19:g.1106409A>G (hg19) ; chr19:g.1106410A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106410A>G , CM000681.2:g.1106410A>G	GRCh38
NC_000019.9:g.1106409A>G , CM000681.1:g.1106409A>G	GRCh37
NC_000019.8:g.1057409A>G	NCBI36
NG_050621.1:g.7485A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.623A>G	ENSP00000473614.3:p.Asp208Gly
ENST00000593032.6:c.492A>G	ENSP00000465828.4:p.Arg164=
ENST00000706713.1:c.506A>G	ENSP00000516510.1:p.Asp169Gly
ENST00000706714.1:c.492A>G	ENSP00000516511.1:p.Arg164=
ENST00000706715.1:c.128A>G	ENSP00000516512.1:p.Asp43Gly
ENST00000354171.13:c.512A>G MANE Select	ENSP00000346103.7:p.Asp171Gly
ENST00000589115.6:c.487A>G	ENSP00000466872.3:p.Thr163Ala
ENST00000354171.12:c.512A>G	ENSP00000346103.7:p.Asp171Gly
ENST00000585480.1:c.245A>G	ENSP00000467900.1:p.Asp82Gly
ENST00000587648.5:c.392A>G	ENSP00000468349.1:p.Asp131Gly
ENST00000588919.5:c.453A>G	ENSP00000464989.3:p.Arg151=
ENST00000589115.5:c.487A>G	ENSP00000466872.2:p.Thr163Ala
ENST00000592940.2:n.883A>G
ENST00000593032.5:c.492A>G	ENSP00000465828.3:p.Arg164=
ENST00000611653.4:c.431A>G	ENSP00000483655.1:p.Asp144Gly
ENST00000616066.4:c.509A>G	ENSP00000485000.1:p.Asp170Gly
ENST00000622390.4:c.620A>G	ENSP00000477503.1:p.Asp207Gly
NM_001039847.2:c.534A>G	NP_001034936.1:p.Arg178=
NM_001039848.2:c.623A>G	NP_001034937.1:p.Asp208Gly
NM_002085.4:c.512A>G	NP_002076.2:p.Asp171Gly
NM_001039848.3:c.623A>G	NP_001034937.1:p.Asp208Gly
NM_001039847.3:c.534A>G	NP_001034936.1:p.Arg178=
NM_001039848.4:c.623A>G	NP_001034937.1:p.Asp208Gly
NM_001367832.1:c.431A>G	NP_001354761.1:p.Asp144Gly
NM_002085.5:c.512A>G MANE Select	NP_002076.2:p.Asp171Gly