Canonical Allele Identifier: CA2317520644

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106408C= , CM000681.2:g.1106408C=	GRCh38
NC_000019.9:g.1106407C= , CM000681.1:g.1106407C=	GRCh37
NC_000019.8:g.1057407C=	NCBI36
NG_050621.1:g.7483C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.621C=	ENSP00000473614.3:p.Ile207=
ENST00000593032.6:c.490C=	ENSP00000465828.4:p.Arg164=
ENST00000706713.1:c.504C=	ENSP00000516510.1:p.Ile168=
ENST00000706714.1:c.490C=	ENSP00000516511.1:p.Arg164=
ENST00000706715.1:c.126C=	ENSP00000516512.1:p.Ile42=
ENST00000354171.13:c.510C= MANE Select	ENSP00000346103.7:p.Ile170=
ENST00000589115.6:c.485C=	ENSP00000466872.3:p.Ser162=
ENST00000354171.12:c.510C=	ENSP00000346103.7:p.Ile170=
ENST00000585480.1:c.243C=	ENSP00000467900.1:p.Ile81=
ENST00000587648.5:c.390C=	ENSP00000468349.1:p.Ile130=
ENST00000588919.5:c.451C=	ENSP00000464989.3:p.Arg151=
ENST00000589115.5:c.485C=	ENSP00000466872.2:p.Ser162=
ENST00000592940.2:n.881C=
ENST00000593032.5:c.490C=	ENSP00000465828.3:p.Arg164=
ENST00000611653.4:c.429C=	ENSP00000483655.1:p.Ile143=
ENST00000616066.4:c.507C=	ENSP00000485000.1:p.Ile169=
ENST00000622390.4:c.618C=	ENSP00000477503.1:p.Ile206=
NM_001039847.2:c.532C=	NP_001034936.1:p.Arg178=
NM_001039848.2:c.621C=	NP_001034937.1:p.Ile207=
NM_002085.4:c.510C=	NP_002076.2:p.Ile170=
NM_001039848.3:c.621C=	NP_001034937.1:p.Ile207=
NM_001039847.3:c.532C=	NP_001034936.1:p.Arg178=
NM_001039848.4:c.621C=	NP_001034937.1:p.Ile207=
NM_001367832.1:c.429C=	NP_001354761.1:p.Ile143=
NM_002085.5:c.510C= MANE Select	NP_002076.2:p.Ile170=