Canonical Allele Identifier: CA402939674
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106405C>A , CM000681.2:g.1106405C>A GRCh38
NC_000019.9:g.1106404C>A , CM000681.1:g.1106404C>A GRCh37
NC_000019.8:g.1057404C>A NCBI36
NG_050621.1:g.7480C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.618C>A ENSP00000473614.3:p.Leu206=
ENST00000593032.6:c.487C>A ENSP00000465828.4:p.His163Asn
ENST00000706713.1:c.501C>A ENSP00000516510.1:p.Leu167=
ENST00000706714.1:c.487C>A ENSP00000516511.1:p.His163Asn
ENST00000706715.1:c.123C>A ENSP00000516512.1:p.Leu41=
ENST00000354171.13:c.507C>A MANE Select ENSP00000346103.7:p.Leu169=
ENST00000589115.6:c.482C>A ENSP00000466872.3:p.Ser161Ter
ENST00000354171.12:c.507C>A ENSP00000346103.7:p.Leu169=
ENST00000585480.1:c.240C>A ENSP00000467900.1:p.Leu80=
ENST00000587648.5:c.387C>A ENSP00000468349.1:p.Leu129=
ENST00000588919.5:c.448C>A ENSP00000464989.3:p.His150Asn
ENST00000589115.5:c.482C>A ENSP00000466872.2:p.Ser161Ter
ENST00000592940.2:n.878C>A
ENST00000593032.5:c.487C>A ENSP00000465828.3:p.His163Asn
ENST00000611653.4:c.426C>A ENSP00000483655.1:p.Leu142=
ENST00000616066.4:c.504C>A ENSP00000485000.1:p.Leu168=
ENST00000622390.4:c.615C>A ENSP00000477503.1:p.Leu205=
NM_001039847.2:c.529C>A NP_001034936.1:p.His177Asn
NM_001039848.2:c.618C>A NP_001034937.1:p.Leu206=
NM_002085.4:c.507C>A NP_002076.2:p.Leu169=
NM_001039848.3:c.618C>A NP_001034937.1:p.Leu206=
NM_001039847.3:c.529C>A NP_001034936.1:p.His177Asn
NM_001039848.4:c.618C>A NP_001034937.1:p.Leu206=
NM_001367832.1:c.426C>A NP_001354761.1:p.Leu142=
NM_002085.5:c.507C>A MANE Select NP_002076.2:p.Leu169=