Canonical Allele Identifier: CA402939103

Gene: GPX4

Linked Data

• dbSNP Id: rs779529317
• MyVariant Identifiers: chr19:g.1106243C>G (hg19) ; chr19:g.1106244C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106244C>G , CM000681.2:g.1106244C>G	GRCh38
NC_000019.9:g.1106243C>G , CM000681.1:g.1106243C>G	GRCh37
NC_000019.8:g.1057243C>G	NCBI36
NG_050621.1:g.7319C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.590C>G	ENSP00000473614.3:p.Ala197Gly
ENST00000593032.6:c.459C>G	ENSP00000465828.4:p.Cys153Trp
ENST00000706713.1:c.473C>G	ENSP00000516510.1:p.Ala158Gly
ENST00000706714.1:c.459C>G	ENSP00000516511.1:p.Cys153Trp
ENST00000706715.1:c.95C>G	ENSP00000516512.1:p.Ala32Gly
ENST00000354171.13:c.479C>G MANE Select	ENSP00000346103.7:p.Ala160Gly
ENST00000589115.6:c.477-156C>G	ENSP00000466872.3:n.477-156C>G
ENST00000354171.12:c.479C>G	ENSP00000346103.7:p.Ala160Gly
ENST00000585480.1:c.212C>G	ENSP00000467900.1:p.Ala71Gly
ENST00000587648.5:c.359C>G	ENSP00000468349.1:p.Ala120Gly
ENST00000588919.5:c.398C>G	ENSP00000464989.3:p.Ala133Gly
ENST00000589115.5:c.477-156C>G	ENSP00000466872.2:n.477-156C>G
ENST00000592940.2:n.850C>G
ENST00000593032.5:c.459C>G	ENSP00000465828.3:p.Cys153Trp
ENST00000611653.4:c.398C>G	ENSP00000483655.1:p.Ala133Gly
ENST00000616066.4:c.476C>G	ENSP00000485000.1:p.Ala159Gly
ENST00000622390.4:c.587C>G	ENSP00000477503.1:p.Ala196Gly
NM_001039847.2:c.479C>G	NP_001034936.1:p.Ala160Gly
NM_001039848.2:c.590C>G	NP_001034937.1:p.Ala197Gly
NM_002085.4:c.479C>G	NP_002076.2:p.Ala160Gly
NM_001039848.3:c.590C>G	NP_001034937.1:p.Ala197Gly
NM_001039847.3:c.479C>G	NP_001034936.1:p.Ala160Gly
NM_001039848.4:c.590C>G	NP_001034937.1:p.Ala197Gly
NM_001367832.1:c.398C>G	NP_001354761.1:p.Ala133Gly
NM_002085.5:c.479C>G MANE Select	NP_002076.2:p.Ala160Gly