Canonical Allele Identifier: CA402940069

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106440A>C (hg19) ; chr19:g.1106441A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106441A>C , CM000681.2:g.1106441A>C	GRCh38
NC_000019.9:g.1106440A>C , CM000681.1:g.1106440A>C	GRCh37
NC_000019.8:g.1057440A>C	NCBI36
NG_050621.1:g.7516A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.654A>C	ENSP00000473614.3:p.Gly218=
ENST00000593032.6:c.523A>C	ENSP00000465828.4:p.Thr175Pro
ENST00000706713.1:c.537A>C	ENSP00000516510.1:p.Gly179=
ENST00000706714.1:c.523A>C	ENSP00000516511.1:p.Thr175Pro
ENST00000706715.1:c.159A>C	ENSP00000516512.1:p.Gly53=
ENST00000354171.13:c.543A>C MANE Select	ENSP00000346103.7:p.Gly181=
ENST00000589115.6:c.518A>C	ENSP00000466872.3:p.Asp173Ala
ENST00000354171.12:c.543A>C	ENSP00000346103.7:p.Gly181=
ENST00000585480.1:c.276A>C	ENSP00000467900.1:p.Gly92=
ENST00000587648.5:c.423A>C	ENSP00000468349.1:p.Gly141=
ENST00000588919.5:c.484A>C	ENSP00000464989.3:p.Thr162Pro
ENST00000589115.5:c.518A>C	ENSP00000466872.2:p.Asp173Ala
ENST00000592940.2:n.914A>C
ENST00000593032.5:c.523A>C	ENSP00000465828.3:p.Thr175Pro
ENST00000611653.4:c.462A>C	ENSP00000483655.1:p.Gly154=
ENST00000616066.4:c.540A>C	ENSP00000485000.1:p.Gly180=
ENST00000622390.4:c.651A>C	ENSP00000477503.1:p.Gly217=
NM_001039847.2:c.565A>C	NP_001034936.1:p.Thr189Pro
NM_001039848.2:c.654A>C	NP_001034937.1:p.Gly218=
NM_002085.4:c.543A>C	NP_002076.2:p.Gly181=
NM_001039848.3:c.654A>C	NP_001034937.1:p.Gly218=
NM_001039847.3:c.565A>C	NP_001034936.1:p.Thr189Pro
NM_001039848.4:c.654A>C	NP_001034937.1:p.Gly218=
NM_001367832.1:c.462A>C	NP_001354761.1:p.Gly154=
NM_002085.5:c.543A>C MANE Select	NP_002076.2:p.Gly181=