Canonical Allele Identifier: CA2317520645

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106409G= , CM000681.2:g.1106409G=	GRCh38
NC_000019.9:g.1106408G= , CM000681.1:g.1106408G=	GRCh37
NC_000019.8:g.1057408G=	NCBI36
NG_050621.1:g.7484G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.622G=	ENSP00000473614.3:p.Asp208=
ENST00000593032.6:c.491G=	ENSP00000465828.4:p.Arg164=
ENST00000706713.1:c.505G=	ENSP00000516510.1:p.Asp169=
ENST00000706714.1:c.491G=	ENSP00000516511.1:p.Arg164=
ENST00000706715.1:c.127G=	ENSP00000516512.1:p.Asp43=
ENST00000354171.13:c.511G= MANE Select	ENSP00000346103.7:p.Asp171=
ENST00000589115.6:c.486G=	ENSP00000466872.3:p.Ser162=
ENST00000354171.12:c.511G=	ENSP00000346103.7:p.Asp171=
ENST00000585480.1:c.244G=	ENSP00000467900.1:p.Asp82=
ENST00000587648.5:c.391G=	ENSP00000468349.1:p.Asp131=
ENST00000588919.5:c.452G=	ENSP00000464989.3:p.Arg151=
ENST00000589115.5:c.486G=	ENSP00000466872.2:p.Ser162=
ENST00000592940.2:n.882G=
ENST00000593032.5:c.491G=	ENSP00000465828.3:p.Arg164=
ENST00000611653.4:c.430G=	ENSP00000483655.1:p.Asp144=
ENST00000616066.4:c.508G=	ENSP00000485000.1:p.Asp170=
ENST00000622390.4:c.619G=	ENSP00000477503.1:p.Asp207=
NM_001039847.2:c.533G=	NP_001034936.1:p.Arg178=
NM_001039848.2:c.622G=	NP_001034937.1:p.Asp208=
NM_002085.4:c.511G=	NP_002076.2:p.Asp171=
NM_001039848.3:c.622G=	NP_001034937.1:p.Asp208=
NM_001039847.3:c.533G=	NP_001034936.1:p.Arg178=
NM_001039848.4:c.622G=	NP_001034937.1:p.Asp208=
NM_001367832.1:c.430G=	NP_001354761.1:p.Asp144=
NM_002085.5:c.511G= MANE Select	NP_002076.2:p.Asp171=