Canonical Allele Identifier: CA402934201
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs945018469
gnomAD v2: 19-1104077-C-G
gnomAD v3: 19-1104078-C-G
gnomAD v4: 19-1104078-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104078C>G , CM000681.2:g.1104078C>G GRCh38
NC_000019.9:g.1104077C>G , CM000681.1:g.1104077C>G GRCh37
NC_000019.8:g.1055077C>G NCBI36
NG_050621.1:g.5153C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593032.6:c.-47C>G ENSP00000465828.4:n.-47C>G
ENST00000706713.1:c.35C>G ENSP00000516510.1:p.Pro12Arg
ENST00000706714.1:c.-47C>G ENSP00000516511.1:n.-47C>G
ENST00000354171.13:c.35C>G MANE Select ENSP00000346103.7:p.Pro12Arg
ENST00000589115.6:c.35C>G ENSP00000466872.3:p.Pro12Arg
ENST00000354171.12:c.35C>G ENSP00000346103.7:p.Pro12Arg
ENST00000588919.5:c.-47C>G ENSP00000464989.3:n.-47C>G
ENST00000589115.5:c.35C>G ENSP00000466872.2:p.Pro12Arg
ENST00000593032.5:c.-47C>G ENSP00000465828.3:n.-47C>G
ENST00000611653.4:c.-47C>G ENSP00000483655.1:n.-47C>G
ENST00000616066.4:c.35C>G ENSP00000485000.1:p.Pro12Arg
NM_001039847.2:c.35C>G NP_001034936.1:p.Pro12Arg
NM_002085.4:c.35C>G NP_002076.2:p.Pro12Arg
NM_001039847.3:c.35C>G NP_001034936.1:p.Pro12Arg
NM_001367832.1:c.-47C>G NP_001354761.1:n.-47C>G
NM_002085.5:c.35C>G MANE Select NP_002076.2:p.Pro12Arg