Canonical Allele Identifier: CA2576544970
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1104008-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104008C>A , CM000681.2:g.1104008C>A GRCh38
NC_000019.9:g.1104007C>A , CM000681.1:g.1104007C>A GRCh37
NC_000019.8:g.1055007C>A NCBI36
NG_050621.1:g.5083C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-36C>A ENSP00000516510.1:n.-36C>A
ENST00000354171.13:c.-36C>A MANE Select ENSP00000346103.7:n.-36C>A
ENST00000589115.6:c.-36C>A ENSP00000466872.3:n.-36C>A
ENST00000354171.12:c.-36C>A ENSP00000346103.7:n.-36C>A
ENST00000589115.5:c.-36C>A ENSP00000466872.2:n.-36C>A
ENST00000616066.4:c.-36C>A ENSP00000485000.1:n.-36C>A
NM_001039847.2:c.-36C>A NP_001034936.1:n.-36C>A
NM_002085.4:c.-36C>A NP_002076.2:n.-36C>A
NM_001039847.3:c.-36C>A NP_001034936.1:n.-36C>A
NM_002085.5:c.-36C>A MANE Select NP_002076.2:n.-36C>A
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