Canonical Allele Identifier: CA2317520729

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106529C= , CM000681.2:g.1106529C=	GRCh38
NC_000019.9:g.1106528C= , CM000681.1:g.1106528C=	GRCh37
NC_000019.8:g.1057528C=	NCBI36
NG_050621.1:g.7604C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.673-11C=	ENSP00000473614.3:n.673-11C=
ENST00000593032.6:c.542-11C=	ENSP00000465828.4:n.542-11C=
ENST00000706713.1:c.556-11C=	ENSP00000516510.1:n.556-11C=
ENST00000706714.1:c.542-11C=	ENSP00000516511.1:n.542-11C=
ENST00000706715.1:c.178-11C=	ENSP00000516512.1:n.178-11C=
ENST00000354171.13:c.562-11C= MANE Select	ENSP00000346103.7:n.562-11C=
ENST00000589115.6:c.537-11C=	ENSP00000466872.3:n.537-11C=
ENST00000354171.12:c.562-11C=	ENSP00000346103.7:n.562-11C=
ENST00000585480.1:c.295-44C=	ENSP00000467900.1:n.295-44C=
ENST00000587648.5:c.442-11C=	ENSP00000468349.1:n.442-11C=
ENST00000588919.5:c.503-11C=	ENSP00000464989.3:n.503-11C=
ENST00000589115.5:c.537-11C=	ENSP00000466872.2:n.537-11C=
ENST00000592940.2:n.933-11C=
ENST00000611653.4:c.481-11C=	ENSP00000483655.1:n.481-11C=
ENST00000616066.4:c.559-11C=	ENSP00000485000.1:n.559-11C=
ENST00000622390.4:c.670-11C=	ENSP00000477503.1:n.670-11C=
NM_001039847.2:c.584-11C=	NP_001034936.1:n.584-11C=
NM_001039848.2:c.673-11C=	NP_001034937.1:n.673-11C=
NM_002085.4:c.562-11C=	NP_002076.2:n.562-11C=
NM_001039848.3:c.673-11C=	NP_001034937.1:n.673-11C=
NM_001039847.3:c.584-11C=	NP_001034936.1:n.584-11C=
NM_001039848.4:c.673-11C=	NP_001034937.1:n.673-11C=
NM_001367832.1:c.481-11C=	NP_001354761.1:n.481-11C=
NM_002085.5:c.562-11C= MANE Select	NP_002076.2:n.562-11C=