Canonical Allele Identifier: CA402937542

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105730T>G (hg19) ; chr19:g.1105731T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105731T>G , CM000681.2:g.1105731T>G	GRCh38
NC_000019.9:g.1105730T>G , CM000681.1:g.1105730T>G	GRCh37
NC_000019.8:g.1056730T>G	NCBI36
NG_050621.1:g.6806T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.509T>G	ENSP00000473614.3:p.Ile170Ser
ENST00000593032.6:c.317T>G	ENSP00000465828.4:p.Ile106Ser
ENST00000706713.1:c.392T>G	ENSP00000516510.1:p.Ile131Ser
ENST00000706714.1:c.317T>G	ENSP00000516511.1:p.Ile106Ser
ENST00000706715.1:c.14T>G	ENSP00000516512.1:p.Ile5Ser
ENST00000354171.13:c.398T>G MANE Select	ENSP00000346103.7:p.Ile133Ser
ENST00000589115.6:c.398T>G	ENSP00000466872.3:p.Ile133Ser
ENST00000354171.12:c.398T>G	ENSP00000346103.7:p.Ile133Ser
ENST00000585362.6:c.509T>G	ENSP00000473614.2:p.Ile170Ser
ENST00000585480.1:c.131T>G	ENSP00000467900.1:p.Ile44Ser
ENST00000587648.5:c.278T>G	ENSP00000468349.1:p.Ile93Ser
ENST00000588919.5:c.317T>G	ENSP00000464989.3:p.Ile106Ser
ENST00000589115.5:c.398T>G	ENSP00000466872.2:p.Ile133Ser
ENST00000592940.2:n.337T>G
ENST00000593032.5:c.317T>G	ENSP00000465828.3:p.Ile106Ser
ENST00000611653.4:c.317T>G	ENSP00000483655.1:p.Ile106Ser
ENST00000616066.4:c.395T>G	ENSP00000485000.1:p.Ile132Ser
ENST00000622390.4:c.506T>G	ENSP00000477503.1:p.Ile169Ser
NM_001039847.2:c.398T>G	NP_001034936.1:p.Ile133Ser
NM_001039848.2:c.509T>G	NP_001034937.1:p.Ile170Ser
NM_002085.4:c.398T>G	NP_002076.2:p.Ile133Ser
NM_001039848.3:c.509T>G	NP_001034937.1:p.Ile170Ser
NM_001039847.3:c.398T>G	NP_001034936.1:p.Ile133Ser
NM_001039848.4:c.509T>G	NP_001034937.1:p.Ile170Ser
NM_001367832.1:c.317T>G	NP_001354761.1:p.Ile106Ser
NM_002085.5:c.398T>G MANE Select	NP_002076.2:p.Ile133Ser