Canonical Allele Identifier: CA402940164

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106454C>A (hg19) ; chr19:g.1106455C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106455C>A , CM000681.2:g.1106455C>A	GRCh38
NC_000019.9:g.1106454C>A , CM000681.1:g.1106454C>A	GRCh37
NC_000019.8:g.1057454C>A	NCBI36
NG_050621.1:g.7530C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.668C>A	ENSP00000473614.3:p.Pro223His
ENST00000593032.6:c.537C>A	ENSP00000465828.4:p.Ala179=
ENST00000706713.1:c.551C>A	ENSP00000516510.1:p.Pro184His
ENST00000706714.1:c.537C>A	ENSP00000516511.1:p.Ala179=
ENST00000706715.1:c.173C>A	ENSP00000516512.1:p.Pro58His
ENST00000354171.13:c.557C>A MANE Select	ENSP00000346103.7:p.Pro186His
ENST00000589115.6:c.532C>A	ENSP00000466872.3:p.Pro178Thr
ENST00000354171.12:c.557C>A	ENSP00000346103.7:p.Pro186His
ENST00000585480.1:c.290C>A	ENSP00000467900.1:p.Pro97His
ENST00000587648.5:c.437C>A	ENSP00000468349.1:p.Pro146His
ENST00000588919.5:c.498C>A	ENSP00000464989.3:p.Ala166=
ENST00000589115.5:c.532C>A	ENSP00000466872.2:p.Pro178Thr
ENST00000592940.2:n.928C>A
ENST00000611653.4:c.476C>A	ENSP00000483655.1:p.Pro159His
ENST00000616066.4:c.554C>A	ENSP00000485000.1:p.Pro185His
ENST00000622390.4:c.665C>A	ENSP00000477503.1:p.Pro222His
NM_001039847.2:c.579C>A	NP_001034936.1:p.Ala193=
NM_001039848.2:c.668C>A	NP_001034937.1:p.Pro223His
NM_002085.4:c.557C>A	NP_002076.2:p.Pro186His
NM_001039848.3:c.668C>A	NP_001034937.1:p.Pro223His
NM_001039847.3:c.579C>A	NP_001034936.1:p.Ala193=
NM_001039848.4:c.668C>A	NP_001034937.1:p.Pro223His
NM_001367832.1:c.476C>A	NP_001354761.1:p.Pro159His
NM_002085.5:c.557C>A MANE Select	NP_002076.2:p.Pro186His