Canonical Allele Identifier: CA402939239

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106261C>T (hg19) ; chr19:g.1106262C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106262C>T , CM000681.2:g.1106262C>T	GRCh38
NC_000019.9:g.1106261C>T , CM000681.1:g.1106261C>T	GRCh37
NC_000019.8:g.1057261C>T	NCBI36
NG_050621.1:g.7337C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.608C>T	ENSP00000473614.3:p.Thr203Ile
ENST00000593032.6:c.477C>T	ENSP00000465828.4:p.His159=
ENST00000706713.1:c.491C>T	ENSP00000516510.1:p.Thr164Ile
ENST00000706714.1:c.477C>T	ENSP00000516511.1:p.His159=
ENST00000706715.1:c.113C>T	ENSP00000516512.1:p.Thr38Ile
ENST00000354171.13:c.497C>T MANE Select	ENSP00000346103.7:p.Thr166Ile
ENST00000589115.6:c.477-138C>T	ENSP00000466872.3:n.477-138C>T
ENST00000354171.12:c.497C>T	ENSP00000346103.7:p.Thr166Ile
ENST00000585480.1:c.230C>T	ENSP00000467900.1:p.Thr77Ile
ENST00000587648.5:c.377C>T	ENSP00000468349.1:p.Thr126Ile
ENST00000588919.5:c.416C>T	ENSP00000464989.3:p.Thr139Ile
ENST00000589115.5:c.477-138C>T	ENSP00000466872.2:n.477-138C>T
ENST00000592940.2:n.868C>T
ENST00000593032.5:c.477C>T	ENSP00000465828.3:p.His159=
ENST00000611653.4:c.416C>T	ENSP00000483655.1:p.Thr139Ile
ENST00000616066.4:c.494C>T	ENSP00000485000.1:p.Thr165Ile
ENST00000622390.4:c.605C>T	ENSP00000477503.1:p.Thr202Ile
NM_001039847.2:c.497C>T	NP_001034936.1:p.Thr166Ile
NM_001039848.2:c.608C>T	NP_001034937.1:p.Thr203Ile
NM_002085.4:c.497C>T	NP_002076.2:p.Thr166Ile
NM_001039848.3:c.608C>T	NP_001034937.1:p.Thr203Ile
NM_001039847.3:c.497C>T	NP_001034936.1:p.Thr166Ile
NM_001039848.4:c.608C>T	NP_001034937.1:p.Thr203Ile
NM_001367832.1:c.416C>T	NP_001354761.1:p.Thr139Ile
NM_002085.5:c.497C>T MANE Select	NP_002076.2:p.Thr166Ile