Canonical Allele Identifier: CA402940037

Gene: GPX4

Linked Data

• dbSNP Id: rs1416229761
• gnomAD v2: 19-1106436-A-G
• gnomAD v4: 19-1106437-A-G
• MyVariant Identifiers: chr19:g.1106436A>G (hg19) ; chr19:g.1106437A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106437A>G , CM000681.2:g.1106437A>G	GRCh38
NC_000019.9:g.1106436A>G , CM000681.1:g.1106436A>G	GRCh37
NC_000019.8:g.1057436A>G	NCBI36
NG_050621.1:g.7512A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.650A>G	ENSP00000473614.3:p.Tyr217Cys
ENST00000593032.6:c.519A>G	ENSP00000465828.4:p.Leu173=
ENST00000706713.1:c.533A>G	ENSP00000516510.1:p.Tyr178Cys
ENST00000706714.1:c.519A>G	ENSP00000516511.1:p.Leu173=
ENST00000706715.1:c.155A>G	ENSP00000516512.1:p.Tyr52Cys
ENST00000354171.13:c.539A>G MANE Select	ENSP00000346103.7:p.Tyr180Cys
ENST00000589115.6:c.514A>G	ENSP00000466872.3:p.Thr172Ala
ENST00000354171.12:c.539A>G	ENSP00000346103.7:p.Tyr180Cys
ENST00000585480.1:c.272A>G	ENSP00000467900.1:p.Tyr91Cys
ENST00000587648.5:c.419A>G	ENSP00000468349.1:p.Tyr140Cys
ENST00000588919.5:c.480A>G	ENSP00000464989.3:p.Leu160=
ENST00000589115.5:c.514A>G	ENSP00000466872.2:p.Thr172Ala
ENST00000592940.2:n.910A>G
ENST00000593032.5:c.519A>G	ENSP00000465828.3:p.Leu173=
ENST00000611653.4:c.458A>G	ENSP00000483655.1:p.Tyr153Cys
ENST00000616066.4:c.536A>G	ENSP00000485000.1:p.Tyr179Cys
ENST00000622390.4:c.647A>G	ENSP00000477503.1:p.Tyr216Cys
NM_001039847.2:c.561A>G	NP_001034936.1:p.Leu187=
NM_001039848.2:c.650A>G	NP_001034937.1:p.Tyr217Cys
NM_002085.4:c.539A>G	NP_002076.2:p.Tyr180Cys
NM_001039848.3:c.650A>G	NP_001034937.1:p.Tyr217Cys
NM_001039847.3:c.561A>G	NP_001034936.1:p.Leu187=
NM_001039848.4:c.650A>G	NP_001034937.1:p.Tyr217Cys
NM_001367832.1:c.458A>G	NP_001354761.1:p.Tyr153Cys
NM_002085.5:c.539A>G MANE Select	NP_002076.2:p.Tyr180Cys