Canonical Allele Identifier: CA2317519008

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104032A= , CM000681.2:g.1104032A=	GRCh38
NC_000019.9:g.1104031A= , CM000681.1:g.1104031A=	GRCh37
NC_000019.8:g.1055031A=	NCBI36
NG_050621.1:g.5107A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706713.1:c.-12A=	ENSP00000516510.1:n.-12A=
ENST00000354171.13:c.-12A= MANE Select	ENSP00000346103.7:n.-12A=
ENST00000589115.6:c.-12A=	ENSP00000466872.3:n.-12A=
ENST00000354171.12:c.-12A=	ENSP00000346103.7:n.-12A=
ENST00000589115.5:c.-12A=	ENSP00000466872.2:n.-12A=
ENST00000616066.4:c.-12A=	ENSP00000485000.1:n.-12A=
NM_001039847.2:c.-12A=	NP_001034936.1:n.-12A=
NM_002085.4:c.-12A=	NP_002076.2:n.-12A=
NM_001039847.3:c.-12A=	NP_001034936.1:n.-12A=
NM_002085.5:c.-12A= MANE Select	NP_002076.2:n.-12A=