Canonical Allele Identifier: CA2317519040

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104065C= , CM000681.2:g.1104065C=	GRCh38
NC_000019.9:g.1104064C= , CM000681.1:g.1104064C=	GRCh37
NC_000019.8:g.1055064C=	NCBI36
NG_050621.1:g.5140C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000706713.1:c.22C=	ENSP00000516510.1:p.Arg8=
ENST00000354171.13:c.22C= MANE Select	ENSP00000346103.7:p.Arg8=
ENST00000589115.6:c.22C=	ENSP00000466872.3:p.Arg8=
ENST00000354171.12:c.22C=	ENSP00000346103.7:p.Arg8=
ENST00000589115.5:c.22C=	ENSP00000466872.2:p.Arg8=
ENST00000611653.4:c.-60C=	ENSP00000483655.1:n.-60C=
ENST00000616066.4:c.22C=	ENSP00000485000.1:p.Arg8=
NM_001039847.2:c.22C=	NP_001034936.1:p.Arg8=
NM_002085.4:c.22C=	NP_002076.2:p.Arg8=
NM_001039847.3:c.22C=	NP_001034936.1:p.Arg8=
NM_001367832.1:c.-60C=	NP_001354761.1:n.-60C=
NM_002085.5:c.22C= MANE Select	NP_002076.2:p.Arg8=