Canonical Allele Identifier: CA402937539

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105729A>G (hg19) ; chr19:g.1105730A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105730A>G , CM000681.2:g.1105730A>G	GRCh38
NC_000019.9:g.1105729A>G , CM000681.1:g.1105729A>G	GRCh37
NC_000019.8:g.1056729A>G	NCBI36
NG_050621.1:g.6805A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.508A>G	ENSP00000473614.3:p.Ile170Val
ENST00000593032.6:c.316A>G	ENSP00000465828.4:p.Ile106Val
ENST00000706713.1:c.391A>G	ENSP00000516510.1:p.Ile131Val
ENST00000706714.1:c.316A>G	ENSP00000516511.1:p.Ile106Val
ENST00000706715.1:c.13A>G	ENSP00000516512.1:p.Ile5Val
ENST00000354171.13:c.397A>G MANE Select	ENSP00000346103.7:p.Ile133Val
ENST00000589115.6:c.397A>G	ENSP00000466872.3:p.Ile133Val
ENST00000354171.12:c.397A>G	ENSP00000346103.7:p.Ile133Val
ENST00000585362.6:c.508A>G	ENSP00000473614.2:p.Ile170Val
ENST00000585480.1:c.130A>G	ENSP00000467900.1:p.Ile44Val
ENST00000587648.5:c.277A>G	ENSP00000468349.1:p.Ile93Val
ENST00000588919.5:c.316A>G	ENSP00000464989.3:p.Ile106Val
ENST00000589115.5:c.397A>G	ENSP00000466872.2:p.Ile133Val
ENST00000592940.2:n.336A>G
ENST00000593032.5:c.316A>G	ENSP00000465828.3:p.Ile106Val
ENST00000611653.4:c.316A>G	ENSP00000483655.1:p.Ile106Val
ENST00000616066.4:c.394A>G	ENSP00000485000.1:p.Ile132Val
ENST00000622390.4:c.505A>G	ENSP00000477503.1:p.Ile169Val
NM_001039847.2:c.397A>G	NP_001034936.1:p.Ile133Val
NM_001039848.2:c.508A>G	NP_001034937.1:p.Ile170Val
NM_002085.4:c.397A>G	NP_002076.2:p.Ile133Val
NM_001039848.3:c.508A>G	NP_001034937.1:p.Ile170Val
NM_001039847.3:c.397A>G	NP_001034936.1:p.Ile133Val
NM_001039848.4:c.508A>G	NP_001034937.1:p.Ile170Val
NM_001367832.1:c.316A>G	NP_001354761.1:p.Ile106Val
NM_002085.5:c.397A>G MANE Select	NP_002076.2:p.Ile133Val