Canonical Allele Identifier: CA2317520889
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106784C= , CM000681.2:g.1106784C= GRCh38
NC_000019.9:g.1106783C= , CM000681.1:g.1106783C= GRCh37
NC_000019.8:g.1057783C= NCBI36
NG_050621.1:g.7859C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.*212C= ENSP00000346103.7:n.*212C=
ENST00000588919.5:c.*18C= ENSP00000464989.3:n.*18C=
ENST00000592940.2:n.1177C=
ENST00000616066.4:c.*212C= ENSP00000485000.1:n.*212C=
ENST00000622390.4:c.*212C= ENSP00000477503.1:n.*212C=
NM_001039847.2:c.*144C= NP_001034936.1:n.*144C=
NM_001039848.2:c.*212C= NP_001034937.1:n.*212C=
NM_002085.4:c.*212C= NP_002076.2:n.*212C=
NM_001039848.3:c.*212C= NP_001034937.1:n.*212C=