Canonical Allele Identifier: CA402940105

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106446G>C (hg19) ; chr19:g.1106447G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106447G>C , CM000681.2:g.1106447G>C	GRCh38
NC_000019.9:g.1106446G>C , CM000681.1:g.1106446G>C	GRCh37
NC_000019.8:g.1057446G>C	NCBI36
NG_050621.1:g.7522G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.660G>C	ENSP00000473614.3:p.Met220Ile
ENST00000593032.6:c.529G>C	ENSP00000465828.4:p.Gly177Arg
ENST00000706713.1:c.543G>C	ENSP00000516510.1:p.Met181Ile
ENST00000706714.1:c.529G>C	ENSP00000516511.1:p.Gly177Arg
ENST00000706715.1:c.165G>C	ENSP00000516512.1:p.Met55Ile
ENST00000354171.13:c.549G>C MANE Select	ENSP00000346103.7:p.Met183Ile
ENST00000589115.6:c.524G>C	ENSP00000466872.3:p.Trp175Ser
ENST00000354171.12:c.549G>C	ENSP00000346103.7:p.Met183Ile
ENST00000585480.1:c.282G>C	ENSP00000467900.1:p.Met94Ile
ENST00000587648.5:c.429G>C	ENSP00000468349.1:p.Met143Ile
ENST00000588919.5:c.490G>C	ENSP00000464989.3:p.Gly164Arg
ENST00000589115.5:c.524G>C	ENSP00000466872.2:p.Trp175Ser
ENST00000592940.2:n.920G>C
ENST00000611653.4:c.468G>C	ENSP00000483655.1:p.Met156Ile
ENST00000616066.4:c.546G>C	ENSP00000485000.1:p.Met182Ile
ENST00000622390.4:c.657G>C	ENSP00000477503.1:p.Met219Ile
NM_001039847.2:c.571G>C	NP_001034936.1:p.Gly191Arg
NM_001039848.2:c.660G>C	NP_001034937.1:p.Met220Ile
NM_002085.4:c.549G>C	NP_002076.2:p.Met183Ile
NM_001039848.3:c.660G>C	NP_001034937.1:p.Met220Ile
NM_001039847.3:c.571G>C	NP_001034936.1:p.Gly191Arg
NM_001039848.4:c.660G>C	NP_001034937.1:p.Met220Ile
NM_001367832.1:c.468G>C	NP_001354761.1:p.Met156Ile
NM_002085.5:c.549G>C MANE Select	NP_002076.2:p.Met183Ile