Canonical Allele Identifier: CA2588205793
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104017dup , CM000681.2:g.1104017dup GRCh38
NC_000019.9:g.1104016dup , CM000681.1:g.1104016dup GRCh37
NC_000019.8:g.1055016dup NCBI36
NG_050621.1:g.5092dup

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-27dup ENSP00000516510.1:n.-27dup
ENST00000354171.13:c.-27dup MANE Select ENSP00000346103.7:n.-27dup
ENST00000589115.6:c.-27dup ENSP00000466872.3:n.-27dup
ENST00000354171.12:c.-27dup ENSP00000346103.7:n.-27dup
ENST00000589115.5:c.-27dup ENSP00000466872.2:n.-27dup
ENST00000616066.4:c.-27dup ENSP00000485000.1:n.-27dup
NM_001039847.2:c.-27dup NP_001034936.1:n.-27dup
NM_002085.4:c.-27dup NP_002076.2:n.-27dup
NM_001039847.3:c.-27dup NP_001034936.1:n.-27dup
NM_002085.5:c.-27dup MANE Select NP_002076.2:n.-27dup