Canonical Allele Identifier: CA2317520126

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105757C= , CM000681.2:g.1105757C=	GRCh38
NC_000019.9:g.1105756C= , CM000681.1:g.1105756C=	GRCh37
NC_000019.8:g.1056756C=	NCBI36
NG_050621.1:g.6832C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.535C=	ENSP00000473614.3:p.Pro179=
ENST00000593032.6:c.343C=	ENSP00000465828.4:p.Pro115=
ENST00000706713.1:c.418C=	ENSP00000516510.1:p.Pro140=
ENST00000706714.1:c.343C=	ENSP00000516511.1:p.Pro115=
ENST00000706715.1:c.40C=	ENSP00000516512.1:p.Pro14=
ENST00000354171.13:c.424C= MANE Select	ENSP00000346103.7:p.Pro142=
ENST00000589115.6:c.424C=	ENSP00000466872.3:p.Pro142=
ENST00000354171.12:c.424C=	ENSP00000346103.7:p.Pro142=
ENST00000585362.6:c.535C=	ENSP00000473614.2:p.Pro179=
ENST00000585480.1:c.157C=	ENSP00000467900.1:p.Pro53=
ENST00000587648.5:c.304C=	ENSP00000468349.1:p.Pro102=
ENST00000588919.5:c.343C=	ENSP00000464989.3:p.Pro115=
ENST00000589115.5:c.424C=	ENSP00000466872.2:p.Pro142=
ENST00000592940.2:n.363C=
ENST00000593032.5:c.343C=	ENSP00000465828.3:p.Pro115=
ENST00000611653.4:c.343C=	ENSP00000483655.1:p.Pro115=
ENST00000616066.4:c.421C=	ENSP00000485000.1:p.Pro141=
ENST00000622390.4:c.532C=	ENSP00000477503.1:p.Pro178=
NM_001039847.2:c.424C=	NP_001034936.1:p.Pro142=
NM_001039848.2:c.535C=	NP_001034937.1:p.Pro179=
NM_002085.4:c.424C=	NP_002076.2:p.Pro142=
NM_001039848.3:c.535C=	NP_001034937.1:p.Pro179=
NM_001039847.3:c.424C=	NP_001034936.1:p.Pro142=
NM_001039848.4:c.535C=	NP_001034937.1:p.Pro179=
NM_001367832.1:c.343C=	NP_001354761.1:p.Pro115=
NM_002085.5:c.424C= MANE Select	NP_002076.2:p.Pro142=