Canonical Allele Identifier: CA2317520092

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105697G= , CM000681.2:g.1105697G=	GRCh38
NC_000019.9:g.1105696G= , CM000681.1:g.1105696G=	GRCh37
NC_000019.8:g.1056696G=	NCBI36
NG_050621.1:g.6772G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.475G=	ENSP00000473614.3:p.Gly159=
ENST00000593032.6:c.283G=	ENSP00000465828.4:p.Gly95=
ENST00000706713.1:c.358G=	ENSP00000516510.1:p.Gly120=
ENST00000706714.1:c.283G=	ENSP00000516511.1:p.Gly95=
ENST00000706715.1:c.-21G=	ENSP00000516512.1:n.-21G=
ENST00000354171.13:c.364G= MANE Select	ENSP00000346103.7:p.Gly122=
ENST00000589115.6:c.364G=	ENSP00000466872.3:p.Gly122=
ENST00000354171.12:c.364G=	ENSP00000346103.7:p.Gly122=
ENST00000585362.6:c.475G=	ENSP00000473614.2:p.Gly159=
ENST00000585480.1:c.97G=	ENSP00000467900.1:p.Gly33=
ENST00000587648.5:c.244G=	ENSP00000468349.1:p.Gly82=
ENST00000588919.5:c.283G=	ENSP00000464989.3:p.Gly95=
ENST00000589115.5:c.364G=	ENSP00000466872.2:p.Gly122=
ENST00000592940.2:n.303G=
ENST00000593032.5:c.283G=	ENSP00000465828.3:p.Gly95=
ENST00000611653.4:c.283G=	ENSP00000483655.1:p.Gly95=
ENST00000616066.4:c.361G=	ENSP00000485000.1:p.Gly121=
ENST00000622390.4:c.472G=	ENSP00000477503.1:p.Gly158=
NM_001039847.2:c.364G=	NP_001034936.1:p.Gly122=
NM_001039848.2:c.475G=	NP_001034937.1:p.Gly159=
NM_002085.4:c.364G=	NP_002076.2:p.Gly122=
NM_001039848.3:c.475G=	NP_001034937.1:p.Gly159=
NM_001039847.3:c.364G=	NP_001034936.1:p.Gly122=
NM_001039848.4:c.475G=	NP_001034937.1:p.Gly159=
NM_001367832.1:c.283G=	NP_001354761.1:p.Gly95=
NM_002085.5:c.364G= MANE Select	NP_002076.2:p.Gly122=