Canonical Allele Identifier: CA2576544972
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104013_1104014del , CM000681.2:g.1104013_1104014del GRCh38
NC_000019.9:g.1104012_1104013del , CM000681.1:g.1104012_1104013del GRCh37
NC_000019.8:g.1055012_1055013del NCBI36
NG_050621.1:g.5088_5089del

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-31_-30del ENSP00000516510.1:n.-31_-30del
ENST00000354171.13:c.-31_-30del MANE Select ENSP00000346103.7:n.-31_-30del
ENST00000589115.6:c.-31_-30del ENSP00000466872.3:n.-31_-30del
ENST00000354171.12:c.-31_-30del ENSP00000346103.7:n.-31_-30del
ENST00000589115.5:c.-31_-30del ENSP00000466872.2:n.-31_-30del
ENST00000616066.4:c.-31_-30del ENSP00000485000.1:n.-31_-30del
NM_001039847.2:c.-31_-30del NP_001034936.1:n.-31_-30del
NM_002085.4:c.-31_-30del NP_002076.2:n.-31_-30del
NM_001039847.3:c.-31_-30del NP_001034936.1:n.-31_-30del
NM_002085.5:c.-31_-30del MANE Select NP_002076.2:n.-31_-30del