Canonical Allele Identifier: CA2317520559

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106298T= , CM000681.2:g.1106298T=	GRCh38
NC_000019.9:g.1106297T= , CM000681.1:g.1106297T=	GRCh37
NC_000019.8:g.1057297T=	NCBI36
NG_050621.1:g.7373T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.612+32T=	ENSP00000473614.3:n.612+32T=
ENST00000593032.6:c.481+32T=	ENSP00000465828.4:n.481+32T=
ENST00000706713.1:c.495+32T=	ENSP00000516510.1:n.495+32T=
ENST00000706714.1:c.481+32T=	ENSP00000516511.1:n.481+32T=
ENST00000706715.1:c.117+32T=	ENSP00000516512.1:n.117+32T=
ENST00000354171.13:c.501+32T= MANE Select	ENSP00000346103.7:n.501+32T=
ENST00000589115.6:c.477-102T=	ENSP00000466872.3:n.477-102T=
ENST00000354171.12:c.501+32T=	ENSP00000346103.7:n.501+32T=
ENST00000585480.1:c.234+32T=	ENSP00000467900.1:n.234+32T=
ENST00000587648.5:c.381+32T=	ENSP00000468349.1:n.381+32T=
ENST00000588919.5:c.420+32T=	ENSP00000464989.3:n.420+32T=
ENST00000589115.5:c.477-102T=	ENSP00000466872.2:n.477-102T=
ENST00000592940.2:n.872+32T=
ENST00000593032.5:c.481+32T=	ENSP00000465828.3:n.481+32T=
ENST00000611653.4:c.420+32T=	ENSP00000483655.1:n.420+32T=
ENST00000616066.4:c.498+32T=	ENSP00000485000.1:n.498+32T=
ENST00000622390.4:c.609+32T=	ENSP00000477503.1:n.609+32T=
NM_001039847.2:c.501+32T=	NP_001034936.1:n.501+32T=
NM_001039848.2:c.612+32T=	NP_001034937.1:n.612+32T=
NM_002085.4:c.501+32T=	NP_002076.2:n.501+32T=
NM_001039848.3:c.612+32T=	NP_001034937.1:n.612+32T=
NM_001039847.3:c.501+32T=	NP_001034936.1:n.501+32T=
NM_001039848.4:c.612+32T=	NP_001034937.1:n.612+32T=
NM_001367832.1:c.420+32T=	NP_001354761.1:n.420+32T=
NM_002085.5:c.501+32T= MANE Select	NP_002076.2:n.501+32T=