Canonical Allele Identifier: CA402940098

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106446-T-A
• MyVariant Identifiers: chr19:g.1106445T>A (hg19) ; chr19:g.1106446T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106446T>A , CM000681.2:g.1106446T>A	GRCh38
NC_000019.9:g.1106445T>A , CM000681.1:g.1106445T>A	GRCh37
NC_000019.8:g.1057445T>A	NCBI36
NG_050621.1:g.7521T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.659T>A	ENSP00000473614.3:p.Met220Lys
ENST00000593032.6:c.528T>A	ENSP00000465828.4:p.His176Gln
ENST00000706713.1:c.542T>A	ENSP00000516510.1:p.Met181Lys
ENST00000706714.1:c.528T>A	ENSP00000516511.1:p.His176Gln
ENST00000706715.1:c.164T>A	ENSP00000516512.1:p.Met55Lys
ENST00000354171.13:c.548T>A MANE Select	ENSP00000346103.7:p.Met183Lys
ENST00000589115.6:c.523T>A	ENSP00000466872.3:p.Trp175Arg
ENST00000354171.12:c.548T>A	ENSP00000346103.7:p.Met183Lys
ENST00000585480.1:c.281T>A	ENSP00000467900.1:p.Met94Lys
ENST00000587648.5:c.428T>A	ENSP00000468349.1:p.Met143Lys
ENST00000588919.5:c.489T>A	ENSP00000464989.3:p.His163Gln
ENST00000589115.5:c.523T>A	ENSP00000466872.2:p.Trp175Arg
ENST00000592940.2:n.919T>A
ENST00000611653.4:c.467T>A	ENSP00000483655.1:p.Met156Lys
ENST00000616066.4:c.545T>A	ENSP00000485000.1:p.Met182Lys
ENST00000622390.4:c.656T>A	ENSP00000477503.1:p.Met219Lys
NM_001039847.2:c.570T>A	NP_001034936.1:p.His190Gln
NM_001039848.2:c.659T>A	NP_001034937.1:p.Met220Lys
NM_002085.4:c.548T>A	NP_002076.2:p.Met183Lys
NM_001039848.3:c.659T>A	NP_001034937.1:p.Met220Lys
NM_001039847.3:c.570T>A	NP_001034936.1:p.His190Gln
NM_001039848.4:c.659T>A	NP_001034937.1:p.Met220Lys
NM_001367832.1:c.467T>A	NP_001354761.1:p.Met156Lys
NM_002085.5:c.548T>A MANE Select	NP_002076.2:p.Met183Lys