Canonical Allele Identifier: CA402939892

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106422C>G (hg19) ; chr19:g.1106423C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106423C>G , CM000681.2:g.1106423C>G	GRCh38
NC_000019.9:g.1106422C>G , CM000681.1:g.1106422C>G	GRCh37
NC_000019.8:g.1057422C>G	NCBI36
NG_050621.1:g.7498C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.636C>G	ENSP00000473614.3:p.Cys212Trp
ENST00000593032.6:c.505C>G	ENSP00000465828.4:p.Arg169Gly
ENST00000706713.1:c.519C>G	ENSP00000516510.1:p.Cys173Trp
ENST00000706714.1:c.505C>G	ENSP00000516511.1:p.Arg169Gly
ENST00000706715.1:c.141C>G	ENSP00000516512.1:p.Cys47Trp
ENST00000354171.13:c.525C>G MANE Select	ENSP00000346103.7:p.Cys175Trp
ENST00000589115.6:c.500C>G	ENSP00000466872.3:p.Ala167Gly
ENST00000354171.12:c.525C>G	ENSP00000346103.7:p.Cys175Trp
ENST00000585480.1:c.258C>G	ENSP00000467900.1:p.Cys86Trp
ENST00000587648.5:c.405C>G	ENSP00000468349.1:p.Cys135Trp
ENST00000588919.5:c.466C>G	ENSP00000464989.3:p.Arg156Gly
ENST00000589115.5:c.500C>G	ENSP00000466872.2:p.Ala167Gly
ENST00000592940.2:n.896C>G
ENST00000593032.5:c.505C>G	ENSP00000465828.3:p.Arg169Gly
ENST00000611653.4:c.444C>G	ENSP00000483655.1:p.Cys148Trp
ENST00000616066.4:c.522C>G	ENSP00000485000.1:p.Cys174Trp
ENST00000622390.4:c.633C>G	ENSP00000477503.1:p.Cys211Trp
NM_001039847.2:c.547C>G	NP_001034936.1:p.Arg183Gly
NM_001039848.2:c.636C>G	NP_001034937.1:p.Cys212Trp
NM_002085.4:c.525C>G	NP_002076.2:p.Cys175Trp
NM_001039848.3:c.636C>G	NP_001034937.1:p.Cys212Trp
NM_001039847.3:c.547C>G	NP_001034936.1:p.Arg183Gly
NM_001039848.4:c.636C>G	NP_001034937.1:p.Cys212Trp
NM_001367832.1:c.444C>G	NP_001354761.1:p.Cys148Trp
NM_002085.5:c.525C>G MANE Select	NP_002076.2:p.Cys175Trp