Canonical Allele Identifier: CA2317519027
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104048G= , CM000681.2:g.1104048G= GRCh38
NC_000019.9:g.1104047G= , CM000681.1:g.1104047G= GRCh37
NC_000019.8:g.1055047G= NCBI36
NG_050621.1:g.5123G=

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.5G= ENSP00000516510.1:p.Ser2=
ENST00000354171.13:c.5G= MANE Select ENSP00000346103.7:p.Ser2=
ENST00000589115.6:c.5G= ENSP00000466872.3:p.Ser2=
ENST00000354171.12:c.5G= ENSP00000346103.7:p.Ser2=
ENST00000589115.5:c.5G= ENSP00000466872.2:p.Ser2=
ENST00000616066.4:c.5G= ENSP00000485000.1:p.Ser2=
NM_001039847.2:c.5G= NP_001034936.1:p.Ser2=
NM_002085.4:c.5G= NP_002076.2:p.Ser2=
NM_001039847.3:c.5G= NP_001034936.1:p.Ser2=
NM_002085.5:c.5G= MANE Select NP_002076.2:p.Ser2=