Canonical Allele Identifier: CA2317519088

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104123C= , CM000681.2:g.1104123C=	GRCh38
NC_000019.9:g.1104122C= , CM000681.1:g.1104122C=	GRCh37
NC_000019.8:g.1055122C=	NCBI36
NG_050621.1:g.5198C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593032.6:c.-2C=	ENSP00000465828.4:n.-2C=
ENST00000706713.1:c.80C=	ENSP00000516510.1:p.Thr27=
ENST00000706714.1:c.-2C=	ENSP00000516511.1:n.-2C=
ENST00000354171.13:c.80C= MANE Select	ENSP00000346103.7:p.Thr27=
ENST00000589115.6:c.80C=	ENSP00000466872.3:p.Thr27=
ENST00000354171.12:c.80C=	ENSP00000346103.7:p.Thr27=
ENST00000588919.5:c.-2C=	ENSP00000464989.3:n.-2C=
ENST00000589115.5:c.80C=	ENSP00000466872.2:p.Thr27=
ENST00000593032.5:c.-2C=	ENSP00000465828.3:n.-2C=
ENST00000611653.4:c.-2C=	ENSP00000483655.1:n.-2C=
ENST00000616066.4:c.80C=	ENSP00000485000.1:p.Thr27=
NM_001039847.2:c.80C=	NP_001034936.1:p.Thr27=
NM_002085.4:c.80C=	NP_002076.2:p.Thr27=
NM_001039847.3:c.80C=	NP_001034936.1:p.Thr27=
NM_001367832.1:c.-2C=	NP_001354761.1:n.-2C=
NM_002085.5:c.80C= MANE Select	NP_002076.2:p.Thr27=