Canonical Allele Identifier: CA2317519083

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104118C= , CM000681.2:g.1104118C=	GRCh38
NC_000019.9:g.1104117C= , CM000681.1:g.1104117C=	GRCh37
NC_000019.8:g.1055117C=	NCBI36
NG_050621.1:g.5193C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593032.6:c.-7C=	ENSP00000465828.4:n.-7C=
ENST00000706713.1:c.75C=	ENSP00000516510.1:p.Ala25=
ENST00000706714.1:c.-7C=	ENSP00000516511.1:n.-7C=
ENST00000354171.13:c.75C= MANE Select	ENSP00000346103.7:p.Ala25=
ENST00000589115.6:c.75C=	ENSP00000466872.3:p.Ala25=
ENST00000354171.12:c.75C=	ENSP00000346103.7:p.Ala25=
ENST00000588919.5:c.-7C=	ENSP00000464989.3:n.-7C=
ENST00000589115.5:c.75C=	ENSP00000466872.2:p.Ala25=
ENST00000593032.5:c.-7C=	ENSP00000465828.3:n.-7C=
ENST00000611653.4:c.-7C=	ENSP00000483655.1:n.-7C=
ENST00000616066.4:c.75C=	ENSP00000485000.1:p.Ala25=
NM_001039847.2:c.75C=	NP_001034936.1:p.Ala25=
NM_002085.4:c.75C=	NP_002076.2:p.Ala25=
NM_001039847.3:c.75C=	NP_001034936.1:p.Ala25=
NM_001367832.1:c.-7C=	NP_001354761.1:n.-7C=
NM_002085.5:c.75C= MANE Select	NP_002076.2:p.Ala25=