Canonical Allele Identifier: CA402937588

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105753C>G (hg19) ; chr19:g.1105754C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105754C>G , CM000681.2:g.1105754C>G	GRCh38
NC_000019.9:g.1105753C>G , CM000681.1:g.1105753C>G	GRCh37
NC_000019.8:g.1056753C>G	NCBI36
NG_050621.1:g.6829C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.532C>G	ENSP00000473614.3:p.His178Asp
ENST00000593032.6:c.340C>G	ENSP00000465828.4:p.His114Asp
ENST00000706713.1:c.415C>G	ENSP00000516510.1:p.His139Asp
ENST00000706714.1:c.340C>G	ENSP00000516511.1:p.His114Asp
ENST00000706715.1:c.37C>G	ENSP00000516512.1:p.His13Asp
ENST00000354171.13:c.421C>G MANE Select	ENSP00000346103.7:p.His141Asp
ENST00000589115.6:c.421C>G	ENSP00000466872.3:p.His141Asp
ENST00000354171.12:c.421C>G	ENSP00000346103.7:p.His141Asp
ENST00000585362.6:c.532C>G	ENSP00000473614.2:p.His178Asp
ENST00000585480.1:c.154C>G	ENSP00000467900.1:p.His52Asp
ENST00000587648.5:c.301C>G	ENSP00000468349.1:p.His101Asp
ENST00000588919.5:c.340C>G	ENSP00000464989.3:p.His114Asp
ENST00000589115.5:c.421C>G	ENSP00000466872.2:p.His141Asp
ENST00000592940.2:n.360C>G
ENST00000593032.5:c.340C>G	ENSP00000465828.3:p.His114Asp
ENST00000611653.4:c.340C>G	ENSP00000483655.1:p.His114Asp
ENST00000616066.4:c.418C>G	ENSP00000485000.1:p.His140Asp
ENST00000622390.4:c.529C>G	ENSP00000477503.1:p.His177Asp
NM_001039847.2:c.421C>G	NP_001034936.1:p.His141Asp
NM_001039848.2:c.532C>G	NP_001034937.1:p.His178Asp
NM_002085.4:c.421C>G	NP_002076.2:p.His141Asp
NM_001039848.3:c.532C>G	NP_001034937.1:p.His178Asp
NM_001039847.3:c.421C>G	NP_001034936.1:p.His141Asp
NM_001039848.4:c.532C>G	NP_001034937.1:p.His178Asp
NM_001367832.1:c.340C>G	NP_001354761.1:p.His114Asp
NM_002085.5:c.421C>G MANE Select	NP_002076.2:p.His141Asp