Canonical Allele Identifier: CA402940300

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106540T>G (hg19) ; chr19:g.1106541T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106541T>G , CM000681.2:g.1106541T>G	GRCh38
NC_000019.9:g.1106540T>G , CM000681.1:g.1106540T>G	GRCh37
NC_000019.8:g.1057540T>G	NCBI36
NG_050621.1:g.7616T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.674T>G	ENSP00000473614.3:p.Val225Gly
ENST00000593032.6:c.543T>G	ENSP00000465828.4:p.Gly181=
ENST00000706713.1:c.557T>G	ENSP00000516510.1:p.Val186Gly
ENST00000706714.1:c.543T>G	ENSP00000516511.1:p.Gly181=
ENST00000706715.1:c.179T>G	ENSP00000516512.1:p.Val60Gly
ENST00000354171.13:c.563T>G MANE Select	ENSP00000346103.7:p.Val188Gly
ENST00000589115.6:c.538T>G	ENSP00000466872.3:p.Ter180Gly
ENST00000354171.12:c.563T>G	ENSP00000346103.7:p.Val188Gly
ENST00000585480.1:c.295-32T>G	ENSP00000467900.1:n.295-32T>G
ENST00000587648.5:c.443T>G	ENSP00000468349.1:p.Val148Gly
ENST00000588919.5:c.504T>G	ENSP00000464989.3:p.Gly168=
ENST00000589115.5:c.538T>G	ENSP00000466872.2:p.Ter180Gly
ENST00000592940.2:n.934T>G
ENST00000611653.4:c.482T>G	ENSP00000483655.1:p.Val161Gly
ENST00000616066.4:c.560T>G	ENSP00000485000.1:p.Val187Gly
ENST00000622390.4:c.671T>G	ENSP00000477503.1:p.Val224Gly
NM_001039847.2:c.585T>G	NP_001034936.1:p.Gly195=
NM_001039848.2:c.674T>G	NP_001034937.1:p.Val225Gly
NM_002085.4:c.563T>G	NP_002076.2:p.Val188Gly
NM_001039848.3:c.674T>G	NP_001034937.1:p.Val225Gly
NM_001039847.3:c.585T>G	NP_001034936.1:p.Gly195=
NM_001039848.4:c.674T>G	NP_001034937.1:p.Val225Gly
NM_001367832.1:c.482T>G	NP_001354761.1:p.Val161Gly
NM_002085.5:c.563T>G MANE Select	NP_002076.2:p.Val188Gly