Canonical Allele Identifier: CA9037558

Gene: GPX4

Linked Data

• dbSNP Id: rs764134016
• ExAC: 19:1106627 C / T
• gnomAD v2: 19-1106627-C-T
• gnomAD v3: 19-1106628-C-T
• gnomAD v4: 19-1106628-C-T
• MyVariant Identifiers: chr19:g.1106627C>T (hg19) ; chr19:g.1106628C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106628C>T , CM000681.2:g.1106628C>T	GRCh38
NC_000019.9:g.1106627C>T , CM000681.1:g.1106627C>T	GRCh37
NC_000019.8:g.1057627C>T	NCBI36
NG_050621.1:g.7703C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.*56C>T	ENSP00000473614.3:n.*56C>T
ENST00000593032.6:c.630C>T	ENSP00000465828.4:p.His210=
ENST00000706713.1:c.*56C>T	ENSP00000516510.1:n.*56C>T
ENST00000706714.1:c.630C>T	ENSP00000516511.1:p.His210=
ENST00000706715.1:c.*56C>T	ENSP00000516512.1:n.*56C>T
ENST00000354171.13:c.*56C>T MANE Select	ENSP00000346103.7:n.*56C>T
ENST00000589115.6:c.*82C>T	ENSP00000466872.3:n.*82C>T
ENST00000354171.12:c.*56C>T	ENSP00000346103.7:n.*56C>T
ENST00000585480.1:c.350C>T	ENSP00000467900.1:p.Thr117Ile
ENST00000588919.5:c.591C>T	ENSP00000464989.3:p.His197=
ENST00000589115.5:c.*82C>T	ENSP00000466872.2:n.*82C>T
ENST00000592940.2:n.1021C>T
ENST00000611653.4:c.*56C>T	ENSP00000483655.1:n.*56C>T
ENST00000616066.4:c.*56C>T	ENSP00000485000.1:n.*56C>T
ENST00000622390.4:c.*56C>T	ENSP00000477503.1:n.*56C>T
NM_001039847.2:c.672C>T	NP_001034936.1:p.His224=
NM_001039848.2:c.*56C>T	NP_001034937.1:n.*56C>T
NM_002085.4:c.*56C>T	NP_002076.2:n.*56C>T
NM_001039848.3:c.*56C>T	NP_001034937.1:n.*56C>T
NM_001039847.3:c.672C>T	NP_001034936.1:p.His224=
NM_001039848.4:c.*56C>T	NP_001034937.1:n.*56C>T
NM_001367832.1:c.*56C>T	NP_001354761.1:n.*56C>T
NM_002085.5:c.*56C>T MANE Select	NP_002076.2:n.*56C>T