Canonical Allele Identifier: CA402940395

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106555T>G (hg19) ; chr19:g.1106556T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106556T>G , CM000681.2:g.1106556T>G	GRCh38
NC_000019.9:g.1106555T>G , CM000681.1:g.1106555T>G	GRCh37
NC_000019.8:g.1057555T>G	NCBI36
NG_050621.1:g.7631T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.689T>G	ENSP00000473614.3:p.Leu230Arg
ENST00000593032.6:c.558T>G	ENSP00000465828.4:p.Pro186=
ENST00000706713.1:c.572T>G	ENSP00000516510.1:p.Leu191Arg
ENST00000706714.1:c.558T>G	ENSP00000516511.1:p.Pro186=
ENST00000706715.1:c.194T>G	ENSP00000516512.1:p.Leu65Arg
ENST00000354171.13:c.578T>G MANE Select	ENSP00000346103.7:p.Leu193Arg
ENST00000589115.6:c.*10T>G	ENSP00000466872.3:n.*10T>G
ENST00000354171.12:c.578T>G	ENSP00000346103.7:p.Leu193Arg
ENST00000585480.1:c.295-17T>G	ENSP00000467900.1:n.295-17T>G
ENST00000587648.5:c.458T>G	ENSP00000468349.1:p.Leu153Arg
ENST00000588919.5:c.519T>G	ENSP00000464989.3:p.Pro173=
ENST00000589115.5:c.*10T>G	ENSP00000466872.2:n.*10T>G
ENST00000592940.2:n.949T>G
ENST00000611653.4:c.497T>G	ENSP00000483655.1:p.Leu166Arg
ENST00000616066.4:c.575T>G	ENSP00000485000.1:p.Leu192Arg
ENST00000622390.4:c.686T>G	ENSP00000477503.1:p.Leu229Arg
NM_001039847.2:c.600T>G	NP_001034936.1:p.Pro200=
NM_001039848.2:c.689T>G	NP_001034937.1:p.Leu230Arg
NM_002085.4:c.578T>G	NP_002076.2:p.Leu193Arg
NM_001039848.3:c.689T>G	NP_001034937.1:p.Leu230Arg
NM_001039847.3:c.600T>G	NP_001034936.1:p.Pro200=
NM_001039848.4:c.689T>G	NP_001034937.1:p.Leu230Arg
NM_001367832.1:c.497T>G	NP_001354761.1:p.Leu166Arg
NM_002085.5:c.578T>G MANE Select	NP_002076.2:p.Leu193Arg