Canonical Allele Identifier: CA2317518986
Gene: GPX4 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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