Canonical Allele Identifier: CA2317519038

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104059_1104060delinsCT , CM000681.2:g.1104059_1104060delinsCT	GRCh38
NC_000019.9:g.1104058_1104059delinsCT , CM000681.1:g.1104058_1104059delinsCT	GRCh37
NC_000019.8:g.1055058_1055059delinsCT	NCBI36
NG_050621.1:g.5134_5135delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706713.1:c.16_17delinsCT	ENSP00000516510.1:p.Leu6=
ENST00000354171.13:c.16_17delinsCT MANE Select	ENSP00000346103.7:p.Leu6=
ENST00000589115.6:c.16_17delinsCT	ENSP00000466872.3:p.Leu6=
ENST00000354171.12:c.16_17delinsCT	ENSP00000346103.7:p.Leu6=
ENST00000589115.5:c.16_17delinsCT	ENSP00000466872.2:p.Leu6=
ENST00000611653.4:c.-66_-65delinsCT	ENSP00000483655.1:n.-66_-65delinsCT
ENST00000616066.4:c.16_17delinsCT	ENSP00000485000.1:p.Leu6=
NM_001039847.2:c.16_17delinsCT	NP_001034936.1:p.Leu6=
NM_002085.4:c.16_17delinsCT	NP_002076.2:p.Leu6=
NM_001039847.3:c.16_17delinsCT	NP_001034936.1:p.Leu6=
NM_001367832.1:c.-66_-65delinsCT	NP_001354761.1:n.-66_-65delinsCT
NM_002085.5:c.16_17delinsCT MANE Select	NP_002076.2:p.Leu6=