Canonical Allele Identifier: CA9037460
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs757133049
gnomAD v2: 19-1106393-C-G
gnomAD v4: 19-1106394-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106394C>G , CM000681.2:g.1106394C>G GRCh38
NC_000019.9:g.1106393C>G , CM000681.1:g.1106393C>G GRCh37
NC_000019.8:g.1057393C>G NCBI36
NG_050621.1:g.7469C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.613-6C>G ENSP00000473614.3:n.613-6C>G
ENST00000593032.6:c.482-6C>G ENSP00000465828.4:n.482-6C>G
ENST00000706713.1:c.496-6C>G ENSP00000516510.1:n.496-6C>G
ENST00000706714.1:c.482-6C>G ENSP00000516511.1:n.482-6C>G
ENST00000706715.1:c.118-6C>G ENSP00000516512.1:n.118-6C>G
ENST00000354171.13:c.502-6C>G MANE Select ENSP00000346103.7:n.502-6C>G
ENST00000589115.6:c.477-6C>G ENSP00000466872.3:n.477-6C>G
ENST00000354171.12:c.502-6C>G ENSP00000346103.7:n.502-6C>G
ENST00000585480.1:c.235-6C>G ENSP00000467900.1:n.235-6C>G
ENST00000587648.5:c.382-6C>G ENSP00000468349.1:n.382-6C>G
ENST00000588919.5:c.437C>G ENSP00000464989.3:p.Ser146Cys
ENST00000589115.5:c.477-6C>G ENSP00000466872.2:n.477-6C>G
ENST00000592940.2:n.873-6C>G
ENST00000593032.5:c.482-6C>G ENSP00000465828.3:n.482-6C>G
ENST00000611653.4:c.421-6C>G ENSP00000483655.1:n.421-6C>G
ENST00000616066.4:c.499-6C>G ENSP00000485000.1:n.499-6C>G
ENST00000622390.4:c.610-6C>G ENSP00000477503.1:n.610-6C>G
NM_001039847.2:c.518C>G NP_001034936.1:p.Ser173Cys
NM_001039848.2:c.613-6C>G NP_001034937.1:n.613-6C>G
NM_002085.4:c.502-6C>G NP_002076.2:n.502-6C>G
NM_001039848.3:c.613-6C>G NP_001034937.1:n.613-6C>G
NM_001039847.3:c.518C>G NP_001034936.1:p.Ser173Cys
NM_001039848.4:c.613-6C>G NP_001034937.1:n.613-6C>G
NM_001367832.1:c.421-6C>G NP_001354761.1:n.421-6C>G
NM_002085.5:c.502-6C>G MANE Select NP_002076.2:n.502-6C>G