Canonical Allele Identifier: CA402939256

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106263A>C (hg19) ; chr19:g.1106264A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106264A>C , CM000681.2:g.1106264A>C	GRCh38
NC_000019.9:g.1106263A>C , CM000681.1:g.1106263A>C	GRCh37
NC_000019.8:g.1057263A>C	NCBI36
NG_050621.1:g.7339A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.610A>C	ENSP00000473614.3:p.Lys204Gln
ENST00000593032.6:c.479A>C	ENSP00000465828.4:p.Gln160Pro
ENST00000706713.1:c.493A>C	ENSP00000516510.1:p.Lys165Gln
ENST00000706714.1:c.479A>C	ENSP00000516511.1:p.Gln160Pro
ENST00000706715.1:c.115A>C	ENSP00000516512.1:p.Lys39Gln
ENST00000354171.13:c.499A>C MANE Select	ENSP00000346103.7:p.Lys167Gln
ENST00000589115.6:c.477-136A>C	ENSP00000466872.3:n.477-136A>C
ENST00000354171.12:c.499A>C	ENSP00000346103.7:p.Lys167Gln
ENST00000585480.1:c.232A>C	ENSP00000467900.1:p.Lys78Gln
ENST00000587648.5:c.379A>C	ENSP00000468349.1:p.Lys127Gln
ENST00000588919.5:c.418A>C	ENSP00000464989.3:p.Lys140Gln
ENST00000589115.5:c.477-136A>C	ENSP00000466872.2:n.477-136A>C
ENST00000592940.2:n.870A>C
ENST00000593032.5:c.479A>C	ENSP00000465828.3:p.Gln160Pro
ENST00000611653.4:c.418A>C	ENSP00000483655.1:p.Lys140Gln
ENST00000616066.4:c.496A>C	ENSP00000485000.1:p.Lys166Gln
ENST00000622390.4:c.607A>C	ENSP00000477503.1:p.Lys203Gln
NM_001039847.2:c.499A>C	NP_001034936.1:p.Lys167Gln
NM_001039848.2:c.610A>C	NP_001034937.1:p.Lys204Gln
NM_002085.4:c.499A>C	NP_002076.2:p.Lys167Gln
NM_001039848.3:c.610A>C	NP_001034937.1:p.Lys204Gln
NM_001039847.3:c.499A>C	NP_001034936.1:p.Lys167Gln
NM_001039848.4:c.610A>C	NP_001034937.1:p.Lys204Gln
NM_001367832.1:c.418A>C	NP_001354761.1:p.Lys140Gln
NM_002085.5:c.499A>C MANE Select	NP_002076.2:p.Lys167Gln