Canonical Allele Identifier: CA402940535

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106627C>G (hg19) ; chr19:g.1106628C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.*56C>G	ENSP00000473614.3:n.*56C>G
ENST00000593032.6:c.630C>G	ENSP00000465828.4:p.His210Gln
ENST00000706713.1:c.*56C>G	ENSP00000516510.1:n.*56C>G
ENST00000706714.1:c.630C>G	ENSP00000516511.1:p.His210Gln
ENST00000706715.1:c.*56C>G	ENSP00000516512.1:n.*56C>G
ENST00000354171.13:c.*56C>G MANE Select	ENSP00000346103.7:n.*56C>G
ENST00000589115.6:c.*82C>G	ENSP00000466872.3:n.*82C>G
ENST00000354171.12:c.*56C>G	ENSP00000346103.7:n.*56C>G
ENST00000585480.1:c.350C>G	ENSP00000467900.1:p.Thr117Ser
ENST00000588919.5:c.591C>G	ENSP00000464989.3:p.His197Gln
ENST00000589115.5:c.*82C>G	ENSP00000466872.2:n.*82C>G
ENST00000592940.2:n.1021C>G
ENST00000611653.4:c.*56C>G	ENSP00000483655.1:n.*56C>G
ENST00000616066.4:c.*56C>G	ENSP00000485000.1:n.*56C>G
ENST00000622390.4:c.*56C>G	ENSP00000477503.1:n.*56C>G
NM_001039847.2:c.672C>G	NP_001034936.1:p.His224Gln
NM_001039848.2:c.*56C>G	NP_001034937.1:n.*56C>G
NM_002085.4:c.*56C>G	NP_002076.2:n.*56C>G
NM_001039848.3:c.*56C>G	NP_001034937.1:n.*56C>G
NM_001039847.3:c.672C>G	NP_001034936.1:p.His224Gln
NM_001039848.4:c.*56C>G	NP_001034937.1:n.*56C>G
NM_001367832.1:c.*56C>G	NP_001354761.1:n.*56C>G
NM_002085.5:c.*56C>G MANE Select	NP_002076.2:n.*56C>G