Canonical Allele Identifier: CA402939247

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106263-C-A
• MyVariant Identifiers: chr19:g.1106262C>A (hg19) ; chr19:g.1106263C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106263C>A , CM000681.2:g.1106263C>A	GRCh38
NC_000019.9:g.1106262C>A , CM000681.1:g.1106262C>A	GRCh37
NC_000019.8:g.1057262C>A	NCBI36
NG_050621.1:g.7338C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.609C>A	ENSP00000473614.3:p.Thr203=
ENST00000593032.6:c.478C>A	ENSP00000465828.4:p.Gln160Lys
ENST00000706713.1:c.492C>A	ENSP00000516510.1:p.Thr164=
ENST00000706714.1:c.478C>A	ENSP00000516511.1:p.Gln160Lys
ENST00000706715.1:c.114C>A	ENSP00000516512.1:p.Thr38=
ENST00000354171.13:c.498C>A MANE Select	ENSP00000346103.7:p.Thr166=
ENST00000589115.6:c.477-137C>A	ENSP00000466872.3:n.477-137C>A
ENST00000354171.12:c.498C>A	ENSP00000346103.7:p.Thr166=
ENST00000585480.1:c.231C>A	ENSP00000467900.1:p.Thr77=
ENST00000587648.5:c.378C>A	ENSP00000468349.1:p.Thr126=
ENST00000588919.5:c.417C>A	ENSP00000464989.3:p.Thr139=
ENST00000589115.5:c.477-137C>A	ENSP00000466872.2:n.477-137C>A
ENST00000592940.2:n.869C>A
ENST00000593032.5:c.478C>A	ENSP00000465828.3:p.Gln160Lys
ENST00000611653.4:c.417C>A	ENSP00000483655.1:p.Thr139=
ENST00000616066.4:c.495C>A	ENSP00000485000.1:p.Thr165=
ENST00000622390.4:c.606C>A	ENSP00000477503.1:p.Thr202=
NM_001039847.2:c.498C>A	NP_001034936.1:p.Thr166=
NM_001039848.2:c.609C>A	NP_001034937.1:p.Thr203=
NM_002085.4:c.498C>A	NP_002076.2:p.Thr166=
NM_001039848.3:c.609C>A	NP_001034937.1:p.Thr203=
NM_001039847.3:c.498C>A	NP_001034936.1:p.Thr166=
NM_001039848.4:c.609C>A	NP_001034937.1:p.Thr203=
NM_001367832.1:c.417C>A	NP_001354761.1:p.Thr139=
NM_002085.5:c.498C>A MANE Select	NP_002076.2:p.Thr166=