Canonical Allele Identifier: CA402937354
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1105659A>C , CM000681.2:g.1105659A>C GRCh38
NC_000019.9:g.1105658A>C , CM000681.1:g.1105658A>C GRCh37
NC_000019.8:g.1056658A>C NCBI36
NG_050621.1:g.6734A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.437A>C ENSP00000473614.3:p.Glu146Ala
ENST00000593032.6:c.245A>C ENSP00000465828.4:p.Glu82Ala
ENST00000706713.1:c.320A>C ENSP00000516510.1:p.Glu107Ala
ENST00000706714.1:c.245A>C ENSP00000516511.1:p.Glu82Ala
ENST00000706715.1:c.-59A>C ENSP00000516512.1:n.-59A>C
ENST00000354171.13:c.326A>C MANE Select ENSP00000346103.7:p.Glu109Ala
ENST00000589115.6:c.326A>C ENSP00000466872.3:p.Glu109Ala
ENST00000354171.12:c.326A>C ENSP00000346103.7:p.Glu109Ala
ENST00000585362.6:c.437A>C ENSP00000473614.2:p.Glu146Ala
ENST00000585480.1:c.59A>C ENSP00000467900.1:p.Glu20Ala
ENST00000587648.5:c.206A>C ENSP00000468349.1:p.Glu69Ala
ENST00000587932.2:n.260A>C
ENST00000588919.5:c.245A>C ENSP00000464989.3:p.Glu82Ala
ENST00000589115.5:c.326A>C ENSP00000466872.2:p.Glu109Ala
ENST00000592940.2:n.271-6A>C
ENST00000593032.5:c.245A>C ENSP00000465828.3:p.Glu82Ala
ENST00000611653.4:c.245A>C ENSP00000483655.1:p.Glu82Ala
ENST00000616066.4:c.323A>C ENSP00000485000.1:p.Glu108Ala
ENST00000622390.4:c.434A>C ENSP00000477503.1:p.Glu145Ala
NM_001039847.2:c.326A>C NP_001034936.1:p.Glu109Ala
NM_001039848.2:c.437A>C NP_001034937.1:p.Glu146Ala
NM_002085.4:c.326A>C NP_002076.2:p.Glu109Ala
NM_001039848.3:c.437A>C NP_001034937.1:p.Glu146Ala
NM_001039847.3:c.326A>C NP_001034936.1:p.Glu109Ala
NM_001039848.4:c.437A>C NP_001034937.1:p.Glu146Ala
NM_001367832.1:c.245A>C NP_001354761.1:p.Glu82Ala
NM_002085.5:c.326A>C MANE Select NP_002076.2:p.Glu109Ala