Canonical Allele Identifier: CA402934222
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104091T>A , CM000681.2:g.1104091T>A GRCh38
NC_000019.9:g.1104090T>A , CM000681.1:g.1104090T>A GRCh37
NC_000019.8:g.1055090T>A NCBI36
NG_050621.1:g.5166T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000593032.6:c.-34T>A ENSP00000465828.4:n.-34T>A
ENST00000706713.1:c.48T>A ENSP00000516510.1:p.Cys16Ter
ENST00000706714.1:c.-34T>A ENSP00000516511.1:n.-34T>A
ENST00000354171.13:c.48T>A MANE Select ENSP00000346103.7:p.Cys16Ter
ENST00000589115.6:c.48T>A ENSP00000466872.3:p.Cys16Ter
ENST00000354171.12:c.48T>A ENSP00000346103.7:p.Cys16Ter
ENST00000588919.5:c.-34T>A ENSP00000464989.3:n.-34T>A
ENST00000589115.5:c.48T>A ENSP00000466872.2:p.Cys16Ter
ENST00000593032.5:c.-34T>A ENSP00000465828.3:n.-34T>A
ENST00000611653.4:c.-34T>A ENSP00000483655.1:n.-34T>A
ENST00000616066.4:c.48T>A ENSP00000485000.1:p.Cys16Ter
NM_001039847.2:c.48T>A NP_001034936.1:p.Cys16Ter
NM_002085.4:c.48T>A NP_002076.2:p.Cys16Ter
NM_001039847.3:c.48T>A NP_001034936.1:p.Cys16Ter
NM_001367832.1:c.-34T>A NP_001354761.1:n.-34T>A
NM_002085.5:c.48T>A MANE Select NP_002076.2:p.Cys16Ter