Canonical Allele Identifier: CA2317520646

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106410A= , CM000681.2:g.1106410A=	GRCh38
NC_000019.9:g.1106409A= , CM000681.1:g.1106409A=	GRCh37
NC_000019.8:g.1057409A=	NCBI36
NG_050621.1:g.7485A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.623A=	ENSP00000473614.3:p.Asp208=
ENST00000593032.6:c.492A=	ENSP00000465828.4:p.Arg164=
ENST00000706713.1:c.506A=	ENSP00000516510.1:p.Asp169=
ENST00000706714.1:c.492A=	ENSP00000516511.1:p.Arg164=
ENST00000706715.1:c.128A=	ENSP00000516512.1:p.Asp43=
ENST00000354171.13:c.512A= MANE Select	ENSP00000346103.7:p.Asp171=
ENST00000589115.6:c.487A=	ENSP00000466872.3:p.Thr163=
ENST00000354171.12:c.512A=	ENSP00000346103.7:p.Asp171=
ENST00000585480.1:c.245A=	ENSP00000467900.1:p.Asp82=
ENST00000587648.5:c.392A=	ENSP00000468349.1:p.Asp131=
ENST00000588919.5:c.453A=	ENSP00000464989.3:p.Arg151=
ENST00000589115.5:c.487A=	ENSP00000466872.2:p.Thr163=
ENST00000592940.2:n.883A=
ENST00000593032.5:c.492A=	ENSP00000465828.3:p.Arg164=
ENST00000611653.4:c.431A=	ENSP00000483655.1:p.Asp144=
ENST00000616066.4:c.509A=	ENSP00000485000.1:p.Asp170=
ENST00000622390.4:c.620A=	ENSP00000477503.1:p.Asp207=
NM_001039847.2:c.534A=	NP_001034936.1:p.Arg178=
NM_001039848.2:c.623A=	NP_001034937.1:p.Asp208=
NM_002085.4:c.512A=	NP_002076.2:p.Asp171=
NM_001039848.3:c.623A=	NP_001034937.1:p.Asp208=
NM_001039847.3:c.534A=	NP_001034936.1:p.Arg178=
NM_001039848.4:c.623A=	NP_001034937.1:p.Asp208=
NM_001367832.1:c.431A=	NP_001354761.1:p.Asp144=
NM_002085.5:c.512A= MANE Select	NP_002076.2:p.Asp171=