Canonical Allele Identifier: CA2317520884

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106774A= , CM000681.2:g.1106774A=	GRCh38
NC_000019.9:g.1106773A= , CM000681.1:g.1106773A=	GRCh37
NC_000019.8:g.1057773A=	NCBI36
NG_050621.1:g.7849A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*202A=	ENSP00000473614.3:n.*202A=
ENST00000706713.1:c.*202A=	ENSP00000516510.1:n.*202A=
ENST00000706715.1:c.*202A=	ENSP00000516512.1:n.*202A=
ENST00000354171.13:c.*202A= MANE Select	ENSP00000346103.7:n.*202A=
ENST00000589115.6:c.*228A=	ENSP00000466872.3:n.*228A=
ENST00000354171.12:c.*202A=	ENSP00000346103.7:n.*202A=
ENST00000585480.1:c.496A=	ENSP00000467900.1:p.Asn166=
ENST00000588919.5:c.*8A=	ENSP00000464989.3:n.*8A=
ENST00000589115.5:c.*228A=	ENSP00000466872.2:n.*228A=
ENST00000592940.2:n.1167A=
ENST00000611653.4:c.*202A=	ENSP00000483655.1:n.*202A=
ENST00000616066.4:c.*202A=	ENSP00000485000.1:n.*202A=
ENST00000622390.4:c.*202A=	ENSP00000477503.1:n.*202A=
NM_001039847.2:c.*134A=	NP_001034936.1:n.*134A=
NM_001039848.2:c.*202A=	NP_001034937.1:n.*202A=
NM_002085.4:c.*202A=	NP_002076.2:n.*202A=
NM_001039848.3:c.*202A=	NP_001034937.1:n.*202A=
NM_001039847.3:c.*134A=	NP_001034936.1:n.*134A=
NM_001039848.4:c.*202A=	NP_001034937.1:n.*202A=
NM_001367832.1:c.*202A=	NP_001354761.1:n.*202A=
NM_002085.5:c.*202A= MANE Select	NP_002076.2:n.*202A=