Canonical Allele Identifier: CA2317520704

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106502G= , CM000681.2:g.1106502G=	GRCh38
NC_000019.9:g.1106501G= , CM000681.1:g.1106501G=	GRCh37
NC_000019.8:g.1057501G=	NCBI36
NG_050621.1:g.7577G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.673-38G=	ENSP00000473614.3:n.673-38G=
ENST00000593032.6:c.542-38G=	ENSP00000465828.4:n.542-38G=
ENST00000706713.1:c.556-38G=	ENSP00000516510.1:n.556-38G=
ENST00000706714.1:c.542-38G=	ENSP00000516511.1:n.542-38G=
ENST00000706715.1:c.178-38G=	ENSP00000516512.1:n.178-38G=
ENST00000354171.13:c.562-38G= MANE Select	ENSP00000346103.7:n.562-38G=
ENST00000589115.6:c.537-38G=	ENSP00000466872.3:n.537-38G=
ENST00000354171.12:c.562-38G=	ENSP00000346103.7:n.562-38G=
ENST00000585480.1:c.294+43G=	ENSP00000467900.1:n.294+43G=
ENST00000587648.5:c.442-38G=	ENSP00000468349.1:n.442-38G=
ENST00000588919.5:c.503-38G=	ENSP00000464989.3:n.503-38G=
ENST00000589115.5:c.537-38G=	ENSP00000466872.2:n.537-38G=
ENST00000592940.2:n.933-38G=
ENST00000611653.4:c.481-38G=	ENSP00000483655.1:n.481-38G=
ENST00000616066.4:c.559-38G=	ENSP00000485000.1:n.559-38G=
ENST00000622390.4:c.670-38G=	ENSP00000477503.1:n.670-38G=
NM_001039847.2:c.584-38G=	NP_001034936.1:n.584-38G=
NM_001039848.2:c.673-38G=	NP_001034937.1:n.673-38G=
NM_002085.4:c.562-38G=	NP_002076.2:n.562-38G=
NM_001039848.3:c.673-38G=	NP_001034937.1:n.673-38G=
NM_001039847.3:c.584-38G=	NP_001034936.1:n.584-38G=
NM_001039848.4:c.673-38G=	NP_001034937.1:n.673-38G=
NM_001367832.1:c.481-38G=	NP_001354761.1:n.481-38G=
NM_002085.5:c.562-38G= MANE Select	NP_002076.2:n.562-38G=