Canonical Allele Identifier: CA9037118
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs756060142
gnomAD v2: 19-1104000-G-A
gnomAD v3: 19-1104001-G-A
gnomAD v4: 19-1104001-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104001G>A , CM000681.2:g.1104001G>A GRCh38
NC_000019.9:g.1104000G>A , CM000681.1:g.1104000G>A GRCh37
NC_000019.8:g.1055000G>A NCBI36
NG_050621.1:g.5076G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-43G>A ENSP00000516510.1:n.-43G>A
ENST00000354171.13:c.-43G>A MANE Select ENSP00000346103.7:n.-43G>A
ENST00000354171.12:c.-43G>A ENSP00000346103.7:n.-43G>A
ENST00000616066.4:c.-43G>A ENSP00000485000.1:n.-43G>A
NM_001039847.2:c.-43G>A NP_001034936.1:n.-43G>A
NM_002085.4:c.-43G>A NP_002076.2:n.-43G>A
NM_001039847.3:c.-43G>A NP_001034936.1:n.-43G>A
NM_002085.5:c.-43G>A MANE Select NP_002076.2:n.-43G>A