Canonical Allele Identifier: CA303994442

Gene: GPX4

Linked Data

• dbSNP Id: rs937189170
• MyVariant Identifiers: chr19:g.1106257T>G (hg19) ; chr19:g.1106258T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106258T>G , CM000681.2:g.1106258T>G	GRCh38
NC_000019.9:g.1106257T>G , CM000681.1:g.1106257T>G	GRCh37
NC_000019.8:g.1057257T>G	NCBI36
NG_050621.1:g.7333T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.604T>G	ENSP00000473614.3:p.Phe202Val
ENST00000593032.6:c.473T>G	ENSP00000465828.4:p.Leu158Arg
ENST00000706713.1:c.487T>G	ENSP00000516510.1:p.Phe163Val
ENST00000706714.1:c.473T>G	ENSP00000516511.1:p.Leu158Arg
ENST00000706715.1:c.109T>G	ENSP00000516512.1:p.Phe37Val
ENST00000354171.13:c.493T>G MANE Select	ENSP00000346103.7:p.Phe165Val
ENST00000589115.6:c.477-142T>G	ENSP00000466872.3:n.477-142T>G
ENST00000354171.12:c.493T>G	ENSP00000346103.7:p.Phe165Val
ENST00000585480.1:c.226T>G	ENSP00000467900.1:p.Phe76Val
ENST00000587648.5:c.373T>G	ENSP00000468349.1:p.Phe125Val
ENST00000588919.5:c.412T>G	ENSP00000464989.3:p.Phe138Val
ENST00000589115.5:c.477-142T>G	ENSP00000466872.2:n.477-142T>G
ENST00000592940.2:n.864T>G
ENST00000593032.5:c.473T>G	ENSP00000465828.3:p.Leu158Arg
ENST00000611653.4:c.412T>G	ENSP00000483655.1:p.Phe138Val
ENST00000616066.4:c.490T>G	ENSP00000485000.1:p.Phe164Val
ENST00000622390.4:c.601T>G	ENSP00000477503.1:p.Phe201Val
NM_001039847.2:c.493T>G	NP_001034936.1:p.Phe165Val
NM_001039848.2:c.604T>G	NP_001034937.1:p.Phe202Val
NM_002085.4:c.493T>G	NP_002076.2:p.Phe165Val
NM_001039848.3:c.604T>G	NP_001034937.1:p.Phe202Val
NM_001039847.3:c.493T>G	NP_001034936.1:p.Phe165Val
NM_001039848.4:c.604T>G	NP_001034937.1:p.Phe202Val
NM_001367832.1:c.412T>G	NP_001354761.1:p.Phe138Val
NM_002085.5:c.493T>G MANE Select	NP_002076.2:p.Phe165Val