Canonical Allele Identifier: CA9037534
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs770665061
gnomAD v2: 19-1106579-A-G
gnomAD v4: 19-1106580-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106580A>G , CM000681.2:g.1106580A>G GRCh38
NC_000019.9:g.1106579A>G , CM000681.1:g.1106579A>G GRCh37
NC_000019.8:g.1057579A>G NCBI36
NG_050621.1:g.7655A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.*8A>G ENSP00000473614.3:n.*8A>G
ENST00000593032.6:c.582A>G ENSP00000465828.4:p.Gln194=
ENST00000706713.1:c.*8A>G ENSP00000516510.1:n.*8A>G
ENST00000706714.1:c.582A>G ENSP00000516511.1:p.Gln194=
ENST00000706715.1:c.*8A>G ENSP00000516512.1:n.*8A>G
ENST00000354171.13:c.*8A>G MANE Select ENSP00000346103.7:n.*8A>G
ENST00000589115.6:c.*34A>G ENSP00000466872.3:n.*34A>G
ENST00000354171.12:c.*8A>G ENSP00000346103.7:n.*8A>G
ENST00000585480.1:c.302A>G ENSP00000467900.1:p.Lys101Arg
ENST00000588919.5:c.543A>G ENSP00000464989.3:p.Gln181=
ENST00000589115.5:c.*34A>G ENSP00000466872.2:n.*34A>G
ENST00000592940.2:n.973A>G
ENST00000611653.4:c.*8A>G ENSP00000483655.1:n.*8A>G
ENST00000616066.4:c.*8A>G ENSP00000485000.1:n.*8A>G
ENST00000622390.4:c.*8A>G ENSP00000477503.1:n.*8A>G
NM_001039847.2:c.624A>G NP_001034936.1:p.Gln208=
NM_001039848.2:c.*8A>G NP_001034937.1:n.*8A>G
NM_002085.4:c.*8A>G NP_002076.2:n.*8A>G
NM_001039848.3:c.*8A>G NP_001034937.1:n.*8A>G
NM_001039847.3:c.624A>G NP_001034936.1:p.Gln208=
NM_001039848.4:c.*8A>G NP_001034937.1:n.*8A>G
NM_001367832.1:c.*8A>G NP_001354761.1:n.*8A>G
NM_002085.5:c.*8A>G MANE Select NP_002076.2:n.*8A>G