Canonical Allele Identifier: CA402939053

Gene: GPX4

Linked Data

• ClinVar Variation Id: 2830182
• ClinVar RCV Id: RCV003678651
• MyVariant Identifiers: chr19:g.1106237C>A (hg19) ; chr19:g.1106238C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106238C>A , CM000681.2:g.1106238C>A	GRCh38
NC_000019.9:g.1106237C>A , CM000681.1:g.1106237C>A	GRCh37
NC_000019.8:g.1057237C>A	NCBI36
NG_050621.1:g.7313C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-4C>A	ENSP00000473614.3:n.588-4C>A
ENST00000593032.6:c.453C>A	ENSP00000465828.4:p.Phe151Leu
ENST00000706713.1:c.471-4C>A	ENSP00000516510.1:n.471-4C>A
ENST00000706714.1:c.453C>A	ENSP00000516511.1:p.Phe151Leu
ENST00000706715.1:c.93-4C>A	ENSP00000516512.1:n.93-4C>A
ENST00000354171.13:c.477-4C>A MANE Select	ENSP00000346103.7:n.477-4C>A
ENST00000589115.6:c.477-162C>A	ENSP00000466872.3:n.477-162C>A
ENST00000354171.12:c.477-4C>A	ENSP00000346103.7:n.477-4C>A
ENST00000585480.1:c.210-4C>A	ENSP00000467900.1:n.210-4C>A
ENST00000587648.5:c.357-4C>A	ENSP00000468349.1:n.357-4C>A
ENST00000588919.5:c.396-4C>A	ENSP00000464989.3:n.396-4C>A
ENST00000589115.5:c.477-162C>A	ENSP00000466872.2:n.477-162C>A
ENST00000592940.2:n.844C>A
ENST00000593032.5:c.453C>A	ENSP00000465828.3:p.Phe151Leu
ENST00000611653.4:c.396-4C>A	ENSP00000483655.1:n.396-4C>A
ENST00000616066.4:c.474-4C>A	ENSP00000485000.1:n.474-4C>A
ENST00000622390.4:c.585-4C>A	ENSP00000477503.1:n.585-4C>A
NM_001039847.2:c.477-4C>A	NP_001034936.1:n.477-4C>A
NM_001039848.2:c.588-4C>A	NP_001034937.1:n.588-4C>A
NM_002085.4:c.477-4C>A	NP_002076.2:n.477-4C>A
NM_001039848.3:c.588-4C>A	NP_001034937.1:n.588-4C>A
NM_001039847.3:c.477-4C>A	NP_001034936.1:n.477-4C>A
NM_001039848.4:c.588-4C>A	NP_001034937.1:n.588-4C>A
NM_001367832.1:c.396-4C>A	NP_001354761.1:n.396-4C>A
NM_002085.5:c.477-4C>A MANE Select	NP_002076.2:n.477-4C>A