Canonical Allele Identifier: CA402940590
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1106655-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106655A>C , CM000681.2:g.1106655A>C GRCh38
NC_000019.9:g.1106654A>C , CM000681.1:g.1106654A>C GRCh37
NC_000019.8:g.1057654A>C NCBI36
NG_050621.1:g.7730A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.*83A>C ENSP00000473614.3:n.*83A>C
ENST00000593032.6:c.657A>C ENSP00000465828.4:p.Lys219Asn
ENST00000706713.1:c.*83A>C ENSP00000516510.1:n.*83A>C
ENST00000706714.1:c.657A>C ENSP00000516511.1:p.Lys219Asn
ENST00000706715.1:c.*83A>C ENSP00000516512.1:n.*83A>C
ENST00000354171.13:c.*83A>C MANE Select ENSP00000346103.7:n.*83A>C
ENST00000589115.6:c.*109A>C ENSP00000466872.3:n.*109A>C
ENST00000354171.12:c.*83A>C ENSP00000346103.7:n.*83A>C
ENST00000585480.1:c.377A>C ENSP00000467900.1:p.Asn126Thr
ENST00000588919.5:c.618A>C ENSP00000464989.3:p.Lys206Asn
ENST00000589115.5:c.*109A>C ENSP00000466872.2:n.*109A>C
ENST00000592940.2:n.1048A>C
ENST00000611653.4:c.*83A>C ENSP00000483655.1:n.*83A>C
ENST00000616066.4:c.*83A>C ENSP00000485000.1:n.*83A>C
ENST00000622390.4:c.*83A>C ENSP00000477503.1:n.*83A>C
NM_001039847.2:c.*15A>C NP_001034936.1:n.*15A>C
NM_001039848.2:c.*83A>C NP_001034937.1:n.*83A>C
NM_002085.4:c.*83A>C NP_002076.2:n.*83A>C
NM_001039848.3:c.*83A>C NP_001034937.1:n.*83A>C
NM_001039847.3:c.*15A>C NP_001034936.1:n.*15A>C
NM_001039848.4:c.*83A>C NP_001034937.1:n.*83A>C
NM_001367832.1:c.*83A>C NP_001354761.1:n.*83A>C
NM_002085.5:c.*83A>C MANE Select NP_002076.2:n.*83A>C