Canonical Allele Identifier: CA2317520649

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106414G= , CM000681.2:g.1106414G=	GRCh38
NC_000019.9:g.1106413G= , CM000681.1:g.1106413G=	GRCh37
NC_000019.8:g.1057413G=	NCBI36
NG_050621.1:g.7489G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.627G=	ENSP00000473614.3:p.Lys209=
ENST00000593032.6:c.496G=	ENSP00000465828.4:p.Glu166=
ENST00000706713.1:c.510G=	ENSP00000516510.1:p.Lys170=
ENST00000706714.1:c.496G=	ENSP00000516511.1:p.Glu166=
ENST00000706715.1:c.132G=	ENSP00000516512.1:p.Lys44=
ENST00000354171.13:c.516G= MANE Select	ENSP00000346103.7:p.Lys172=
ENST00000589115.6:c.491G=	ENSP00000466872.3:p.Arg164=
ENST00000354171.12:c.516G=	ENSP00000346103.7:p.Lys172=
ENST00000585480.1:c.249G=	ENSP00000467900.1:p.Lys83=
ENST00000587648.5:c.396G=	ENSP00000468349.1:p.Lys132=
ENST00000588919.5:c.457G=	ENSP00000464989.3:p.Glu153=
ENST00000589115.5:c.491G=	ENSP00000466872.2:p.Arg164=
ENST00000592940.2:n.887G=
ENST00000593032.5:c.496G=	ENSP00000465828.3:p.Glu166=
ENST00000611653.4:c.435G=	ENSP00000483655.1:p.Lys145=
ENST00000616066.4:c.513G=	ENSP00000485000.1:p.Lys171=
ENST00000622390.4:c.624G=	ENSP00000477503.1:p.Lys208=
NM_001039847.2:c.538G=	NP_001034936.1:p.Glu180=
NM_001039848.2:c.627G=	NP_001034937.1:p.Lys209=
NM_002085.4:c.516G=	NP_002076.2:p.Lys172=
NM_001039848.3:c.627G=	NP_001034937.1:p.Lys209=
NM_001039847.3:c.538G=	NP_001034936.1:p.Glu180=
NM_001039848.4:c.627G=	NP_001034937.1:p.Lys209=
NM_001367832.1:c.435G=	NP_001354761.1:p.Lys145=
NM_002085.5:c.516G= MANE Select	NP_002076.2:p.Lys172=