Canonical Allele Identifier: CA2588207843

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106388-G-GTCTCTCCACAGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106389_1106401dup , CM000681.2:g.1106389_1106401dup	GRCh38
NC_000019.9:g.1106388_1106400dup , CM000681.1:g.1106388_1106400dup	GRCh37
NC_000019.8:g.1057388_1057400dup	NCBI36
NG_050621.1:g.7464_7476dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.613-11_614dup
ENST00000593032.6:c.482-11_483dup
ENST00000706713.1:c.496-11_497dup
ENST00000706714.1:c.482-11_483dup
ENST00000706715.1:c.118-11_119dup
ENST00000354171.13:c.502-11_503dup
ENST00000589115.6:c.477-11_478dup
ENST00000354171.12:c.502-11_503dup
ENST00000585480.1:c.235-11_236dup
ENST00000587648.5:c.382-11_383dup
ENST00000588919.5:c.432_444dup	ENSP00000464989.3:p.Pro149SerfsTer14
ENST00000589115.5:c.477-11_478dup
ENST00000592940.2:n.873-11_874dup
ENST00000593032.5:c.482-11_483dup
ENST00000611653.4:c.421-11_422dup
ENST00000616066.4:c.499-11_500dup
ENST00000622390.4:c.610-11_611dup
NM_001039847.2:c.513_525dup	NP_001034936.1:p.Pro176SerfsTer14
NM_001039848.2:c.613-11_614dup
NM_002085.4:c.502-11_503dup
NM_001039848.3:c.613-11_614dup
NM_001039847.3:c.513_525dup	NP_001034936.1:p.Pro176SerfsTer14
NM_001039848.4:c.613-11_614dup
NM_001367832.1:c.421-11_422dup
NM_002085.5:c.502-11_503dup