Canonical Allele Identifier: CA402940356

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106547G>C (hg19) ; chr19:g.1106548G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106548G>C , CM000681.2:g.1106548G>C	GRCh38
NC_000019.9:g.1106547G>C , CM000681.1:g.1106547G>C	GRCh37
NC_000019.8:g.1057547G>C	NCBI36
NG_050621.1:g.7623G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.681G>C	ENSP00000473614.3:p.Glu227Asp
ENST00000593032.6:c.550G>C	ENSP00000465828.4:p.Glu184Gln
ENST00000706713.1:c.564G>C	ENSP00000516510.1:p.Glu188Asp
ENST00000706714.1:c.550G>C	ENSP00000516511.1:p.Glu184Gln
ENST00000706715.1:c.186G>C	ENSP00000516512.1:p.Glu62Asp
ENST00000354171.13:c.570G>C MANE Select	ENSP00000346103.7:p.Glu190Asp
ENST00000589115.6:c.*2G>C	ENSP00000466872.3:n.*2G>C
ENST00000354171.12:c.570G>C	ENSP00000346103.7:p.Glu190Asp
ENST00000585480.1:c.295-25G>C	ENSP00000467900.1:n.295-25G>C
ENST00000587648.5:c.450G>C	ENSP00000468349.1:p.Glu150Asp
ENST00000588919.5:c.511G>C	ENSP00000464989.3:p.Glu171Gln
ENST00000589115.5:c.*2G>C	ENSP00000466872.2:n.*2G>C
ENST00000592940.2:n.941G>C
ENST00000611653.4:c.489G>C	ENSP00000483655.1:p.Glu163Asp
ENST00000616066.4:c.567G>C	ENSP00000485000.1:p.Glu189Asp
ENST00000622390.4:c.678G>C	ENSP00000477503.1:p.Glu226Asp
NM_001039847.2:c.592G>C	NP_001034936.1:p.Glu198Gln
NM_001039848.2:c.681G>C	NP_001034937.1:p.Glu227Asp
NM_002085.4:c.570G>C	NP_002076.2:p.Glu190Asp
NM_001039848.3:c.681G>C	NP_001034937.1:p.Glu227Asp
NM_001039847.3:c.592G>C	NP_001034936.1:p.Glu198Gln
NM_001039848.4:c.681G>C	NP_001034937.1:p.Glu227Asp
NM_001367832.1:c.489G>C	NP_001354761.1:p.Glu163Asp
NM_002085.5:c.570G>C MANE Select	NP_002076.2:p.Glu190Asp