Canonical Allele Identifier: CA9037396

Gene: GPX4

Linked Data

• dbSNP Id: rs774119191
• ExAC: 19:1106196 T / TG
• gnomAD v2: 19-1106196-T-TG
• gnomAD v4: 19-1106197-T-TG
• MyVariant Identifiers: chr19:g.1106196_1106197insG (hg19) ; chr19:g.1106197_1106198insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106203dup , CM000681.2:g.1106203dup	GRCh38
NC_000019.9:g.1106202dup , CM000681.1:g.1106202dup	GRCh37
NC_000019.8:g.1057202dup	NCBI36
NG_050621.1:g.7278dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-39dup	ENSP00000473614.3:n.588-39dup
ENST00000593032.6:c.418dup	ENSP00000465828.4:p.Ala140GlyfsTer?
ENST00000706713.1:c.471-39dup	ENSP00000516510.1:n.471-39dup
ENST00000706714.1:c.418dup	ENSP00000516511.1:p.Ala140GlyfsTer?
ENST00000706715.1:c.93-39dup	ENSP00000516512.1:n.93-39dup
ENST00000354171.13:c.477-39dup MANE Select	ENSP00000346103.7:n.477-39dup
ENST00000589115.6:c.477-197dup	ENSP00000466872.3:n.477-197dup
ENST00000354171.12:c.477-39dup	ENSP00000346103.7:n.477-39dup
ENST00000585480.1:c.210-39dup	ENSP00000467900.1:n.210-39dup
ENST00000587648.5:c.357-39dup	ENSP00000468349.1:n.357-39dup
ENST00000588919.5:c.396-39dup	ENSP00000464989.3:n.396-39dup
ENST00000589115.5:c.477-197dup	ENSP00000466872.2:n.477-197dup
ENST00000592940.2:n.809dup
ENST00000593032.5:c.418dup	ENSP00000465828.3:p.Ala140GlyfsTer?
ENST00000611653.4:c.396-39dup	ENSP00000483655.1:n.396-39dup
ENST00000616066.4:c.474-39dup	ENSP00000485000.1:n.474-39dup
ENST00000622390.4:c.585-39dup	ENSP00000477503.1:n.585-39dup
NM_001039847.2:c.477-39dup	NP_001034936.1:n.477-39dup
NM_001039848.2:c.588-39dup	NP_001034937.1:n.588-39dup
NM_002085.4:c.477-39dup	NP_002076.2:n.477-39dup
NM_001039848.3:c.588-39dup	NP_001034937.1:n.588-39dup
NM_001039847.3:c.477-39dup	NP_001034936.1:n.477-39dup
NM_001039848.4:c.588-39dup	NP_001034937.1:n.588-39dup
NM_001367832.1:c.396-39dup	NP_001354761.1:n.396-39dup
NM_002085.5:c.477-39dup MANE Select	NP_002076.2:n.477-39dup