Canonical Allele Identifier: CA402937660

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105782A>C (hg19) ; chr19:g.1105783A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105783A>C , CM000681.2:g.1105783A>C	GRCh38
NC_000019.9:g.1105782A>C , CM000681.1:g.1105782A>C	GRCh37
NC_000019.8:g.1056782A>C	NCBI36
NG_050621.1:g.6858A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.561A>C	ENSP00000473614.3:p.Gln187His
ENST00000593032.6:c.369A>C	ENSP00000465828.4:p.Gln123His
ENST00000706713.1:c.444A>C	ENSP00000516510.1:p.Gln148His
ENST00000706714.1:c.369A>C	ENSP00000516511.1:p.Gln123His
ENST00000706715.1:c.66A>C	ENSP00000516512.1:p.Gln22His
ENST00000354171.13:c.450A>C MANE Select	ENSP00000346103.7:p.Gln150His
ENST00000589115.6:c.450A>C	ENSP00000466872.3:p.Gln150His
ENST00000354171.12:c.450A>C	ENSP00000346103.7:p.Gln150His
ENST00000585480.1:c.183A>C	ENSP00000467900.1:p.Gln61His
ENST00000587648.5:c.330A>C	ENSP00000468349.1:p.Gln110His
ENST00000588919.5:c.369A>C	ENSP00000464989.3:p.Gln123His
ENST00000589115.5:c.450A>C	ENSP00000466872.2:p.Gln150His
ENST00000592940.2:n.389A>C
ENST00000593032.5:c.369A>C	ENSP00000465828.3:p.Gln123His
ENST00000611653.4:c.369A>C	ENSP00000483655.1:p.Gln123His
ENST00000616066.4:c.447A>C	ENSP00000485000.1:p.Gln149His
ENST00000622390.4:c.558A>C	ENSP00000477503.1:p.Gln186His
NM_001039847.2:c.450A>C	NP_001034936.1:p.Gln150His
NM_001039848.2:c.561A>C	NP_001034937.1:p.Gln187His
NM_002085.4:c.450A>C	NP_002076.2:p.Gln150His
NM_001039848.3:c.561A>C	NP_001034937.1:p.Gln187His
NM_001039847.3:c.450A>C	NP_001034936.1:p.Gln150His
NM_001039848.4:c.561A>C	NP_001034937.1:p.Gln187His
NM_001367832.1:c.369A>C	NP_001354761.1:p.Gln123His
NM_002085.5:c.450A>C MANE Select	NP_002076.2:p.Gln150His