Canonical Allele Identifier: CA402937530

Gene: GPX4

Linked Data

• gnomAD v4: 19-1105726-C-G
• MyVariant Identifiers: chr19:g.1105725C>G (hg19) ; chr19:g.1105726C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105726C>G , CM000681.2:g.1105726C>G	GRCh38
NC_000019.9:g.1105725C>G , CM000681.1:g.1105725C>G	GRCh37
NC_000019.8:g.1056725C>G	NCBI36
NG_050621.1:g.6801C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.504C>G	ENSP00000473614.3:p.Ser168Arg
ENST00000593032.6:c.312C>G	ENSP00000465828.4:p.Ser104Arg
ENST00000706713.1:c.387C>G	ENSP00000516510.1:p.Ser129Arg
ENST00000706714.1:c.312C>G	ENSP00000516511.1:p.Ser104Arg
ENST00000706715.1:c.9C>G	ENSP00000516512.1:p.Ser3Arg
ENST00000354171.13:c.393C>G MANE Select	ENSP00000346103.7:p.Ser131Arg
ENST00000589115.6:c.393C>G	ENSP00000466872.3:p.Ser131Arg
ENST00000354171.12:c.393C>G	ENSP00000346103.7:p.Ser131Arg
ENST00000585362.6:c.504C>G	ENSP00000473614.2:p.Ser168Arg
ENST00000585480.1:c.126C>G	ENSP00000467900.1:p.Ser42Arg
ENST00000587648.5:c.273C>G	ENSP00000468349.1:p.Ser91Arg
ENST00000588919.5:c.312C>G	ENSP00000464989.3:p.Ser104Arg
ENST00000589115.5:c.393C>G	ENSP00000466872.2:p.Ser131Arg
ENST00000592940.2:n.332C>G
ENST00000593032.5:c.312C>G	ENSP00000465828.3:p.Ser104Arg
ENST00000611653.4:c.312C>G	ENSP00000483655.1:p.Ser104Arg
ENST00000616066.4:c.390C>G	ENSP00000485000.1:p.Ser130Arg
ENST00000622390.4:c.501C>G	ENSP00000477503.1:p.Ser167Arg
NM_001039847.2:c.393C>G	NP_001034936.1:p.Ser131Arg
NM_001039848.2:c.504C>G	NP_001034937.1:p.Ser168Arg
NM_002085.4:c.393C>G	NP_002076.2:p.Ser131Arg
NM_001039848.3:c.504C>G	NP_001034937.1:p.Ser168Arg
NM_001039847.3:c.393C>G	NP_001034936.1:p.Ser131Arg
NM_001039848.4:c.504C>G	NP_001034937.1:p.Ser168Arg
NM_001367832.1:c.312C>G	NP_001354761.1:p.Ser104Arg
NM_002085.5:c.393C>G MANE Select	NP_002076.2:p.Ser131Arg