Canonical Allele Identifier: CA2317520887
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106780C= , CM000681.2:g.1106780C= GRCh38
NC_000019.9:g.1106779C= , CM000681.1:g.1106779C= GRCh37
NC_000019.8:g.1057779C= NCBI36
NG_050621.1:g.7855C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706713.1:c.*208C= ENSP00000516510.1:n.*208C=
ENST00000354171.12:c.*208C= ENSP00000346103.7:n.*208C=
ENST00000588919.5:c.*14C= ENSP00000464989.3:n.*14C=
ENST00000592940.2:n.1173C=
ENST00000616066.4:c.*208C= ENSP00000485000.1:n.*208C=
ENST00000622390.4:c.*208C= ENSP00000477503.1:n.*208C=
NM_001039847.2:c.*140C= NP_001034936.1:n.*140C=
NM_001039848.2:c.*208C= NP_001034937.1:n.*208C=
NM_002085.4:c.*208C= NP_002076.2:n.*208C=
NM_001039848.3:c.*208C= NP_001034937.1:n.*208C=