Canonical Allele Identifier: CA402939452

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106378T>C (hg19) ; chr19:g.1106379T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106379T>C , CM000681.2:g.1106379T>C	GRCh38
NC_000019.9:g.1106378T>C , CM000681.1:g.1106378T>C	GRCh37
NC_000019.8:g.1057378T>C	NCBI36
NG_050621.1:g.7454T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.613-21T>C	ENSP00000473614.3:n.613-21T>C
ENST00000593032.6:c.482-21T>C	ENSP00000465828.4:n.482-21T>C
ENST00000706713.1:c.496-21T>C	ENSP00000516510.1:n.496-21T>C
ENST00000706714.1:c.482-21T>C	ENSP00000516511.1:n.482-21T>C
ENST00000706715.1:c.118-21T>C	ENSP00000516512.1:n.118-21T>C
ENST00000354171.13:c.502-21T>C MANE Select	ENSP00000346103.7:n.502-21T>C
ENST00000589115.6:c.477-21T>C	ENSP00000466872.3:n.477-21T>C
ENST00000354171.12:c.502-21T>C	ENSP00000346103.7:n.502-21T>C
ENST00000585480.1:c.235-21T>C	ENSP00000467900.1:n.235-21T>C
ENST00000587648.5:c.382-21T>C	ENSP00000468349.1:n.382-21T>C
ENST00000588919.5:c.422T>C	ENSP00000464989.3:p.Phe141Ser
ENST00000589115.5:c.477-21T>C	ENSP00000466872.2:n.477-21T>C
ENST00000592940.2:n.873-21T>C
ENST00000593032.5:c.482-21T>C	ENSP00000465828.3:n.482-21T>C
ENST00000611653.4:c.421-21T>C	ENSP00000483655.1:n.421-21T>C
ENST00000616066.4:c.499-21T>C	ENSP00000485000.1:n.499-21T>C
ENST00000622390.4:c.610-21T>C	ENSP00000477503.1:n.610-21T>C
NM_001039847.2:c.503T>C	NP_001034936.1:p.Phe168Ser
NM_001039848.2:c.613-21T>C	NP_001034937.1:n.613-21T>C
NM_002085.4:c.502-21T>C	NP_002076.2:n.502-21T>C
NM_001039848.3:c.613-21T>C	NP_001034937.1:n.613-21T>C
NM_001039847.3:c.503T>C	NP_001034936.1:p.Phe168Ser
NM_001039848.4:c.613-21T>C	NP_001034937.1:n.613-21T>C
NM_001367832.1:c.421-21T>C	NP_001354761.1:n.421-21T>C
NM_002085.5:c.502-21T>C MANE Select	NP_002076.2:n.502-21T>C