Canonical Allele Identifier: CA2317520518

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106246A= , CM000681.2:g.1106246A=	GRCh38
NC_000019.9:g.1106245A= , CM000681.1:g.1106245A=	GRCh37
NC_000019.8:g.1057245A=	NCBI36
NG_050621.1:g.7321A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.592A=	ENSP00000473614.3:p.Ile198=
ENST00000593032.6:c.461A=	ENSP00000465828.4:p.His154=
ENST00000706713.1:c.475A=	ENSP00000516510.1:p.Ile159=
ENST00000706714.1:c.461A=	ENSP00000516511.1:p.His154=
ENST00000706715.1:c.97A=	ENSP00000516512.1:p.Ile33=
ENST00000354171.13:c.481A= MANE Select	ENSP00000346103.7:p.Ile161=
ENST00000589115.6:c.477-154A=	ENSP00000466872.3:n.477-154A=
ENST00000354171.12:c.481A=	ENSP00000346103.7:p.Ile161=
ENST00000585480.1:c.214A=	ENSP00000467900.1:p.Ile72=
ENST00000587648.5:c.361A=	ENSP00000468349.1:p.Ile121=
ENST00000588919.5:c.400A=	ENSP00000464989.3:p.Ile134=
ENST00000589115.5:c.477-154A=	ENSP00000466872.2:n.477-154A=
ENST00000592940.2:n.852A=
ENST00000593032.5:c.461A=	ENSP00000465828.3:p.His154=
ENST00000611653.4:c.400A=	ENSP00000483655.1:p.Ile134=
ENST00000616066.4:c.478A=	ENSP00000485000.1:p.Ile160=
ENST00000622390.4:c.589A=	ENSP00000477503.1:p.Ile197=
NM_001039847.2:c.481A=	NP_001034936.1:p.Ile161=
NM_001039848.2:c.592A=	NP_001034937.1:p.Ile198=
NM_002085.4:c.481A=	NP_002076.2:p.Ile161=
NM_001039848.3:c.592A=	NP_001034937.1:p.Ile198=
NM_001039847.3:c.481A=	NP_001034936.1:p.Ile161=
NM_001039848.4:c.592A=	NP_001034937.1:p.Ile198=
NM_001367832.1:c.400A=	NP_001354761.1:p.Ile134=
NM_002085.5:c.481A= MANE Select	NP_002076.2:p.Ile161=