Canonical Allele Identifier: CA402940080

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106441C>G (hg19) ; chr19:g.1106442C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106442C>G , CM000681.2:g.1106442C>G	GRCh38
NC_000019.9:g.1106441C>G , CM000681.1:g.1106441C>G	GRCh37
NC_000019.8:g.1057441C>G	NCBI36
NG_050621.1:g.7517C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.655C>G	ENSP00000473614.3:p.Pro219Ala
ENST00000593032.6:c.524C>G	ENSP00000465828.4:p.Thr175Ser
ENST00000706713.1:c.538C>G	ENSP00000516510.1:p.Pro180Ala
ENST00000706714.1:c.524C>G	ENSP00000516511.1:p.Thr175Ser
ENST00000706715.1:c.160C>G	ENSP00000516512.1:p.Pro54Ala
ENST00000354171.13:c.544C>G MANE Select	ENSP00000346103.7:p.Pro182Ala
ENST00000589115.6:c.519C>G	ENSP00000466872.3:p.Asp173Glu
ENST00000354171.12:c.544C>G	ENSP00000346103.7:p.Pro182Ala
ENST00000585480.1:c.277C>G	ENSP00000467900.1:p.Pro93Ala
ENST00000587648.5:c.424C>G	ENSP00000468349.1:p.Pro142Ala
ENST00000588919.5:c.485C>G	ENSP00000464989.3:p.Thr162Ser
ENST00000589115.5:c.519C>G	ENSP00000466872.2:p.Asp173Glu
ENST00000592940.2:n.915C>G
ENST00000593032.5:c.524C>G	ENSP00000465828.3:p.Thr175Ser
ENST00000611653.4:c.463C>G	ENSP00000483655.1:p.Pro155Ala
ENST00000616066.4:c.541C>G	ENSP00000485000.1:p.Pro181Ala
ENST00000622390.4:c.652C>G	ENSP00000477503.1:p.Pro218Ala
NM_001039847.2:c.566C>G	NP_001034936.1:p.Thr189Ser
NM_001039848.2:c.655C>G	NP_001034937.1:p.Pro219Ala
NM_002085.4:c.544C>G	NP_002076.2:p.Pro182Ala
NM_001039848.3:c.655C>G	NP_001034937.1:p.Pro219Ala
NM_001039847.3:c.566C>G	NP_001034936.1:p.Thr189Ser
NM_001039848.4:c.655C>G	NP_001034937.1:p.Pro219Ala
NM_001367832.1:c.463C>G	NP_001354761.1:p.Pro155Ala
NM_002085.5:c.544C>G MANE Select	NP_002076.2:p.Pro182Ala