Canonical Allele Identifier: CA402940439

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106574C>A (hg19) ; chr19:g.1106575C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106575C>A , CM000681.2:g.1106575C>A	GRCh38
NC_000019.9:g.1106574C>A , CM000681.1:g.1106574C>A	GRCh37
NC_000019.8:g.1057574C>A	NCBI36
NG_050621.1:g.7650C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*3C>A	ENSP00000473614.3:n.*3C>A
ENST00000593032.6:c.577C>A	ENSP00000465828.4:p.Pro193Thr
ENST00000706713.1:c.*3C>A	ENSP00000516510.1:n.*3C>A
ENST00000706714.1:c.577C>A	ENSP00000516511.1:p.Pro193Thr
ENST00000706715.1:c.*3C>A	ENSP00000516512.1:n.*3C>A
ENST00000354171.13:c.*3C>A MANE Select	ENSP00000346103.7:n.*3C>A
ENST00000589115.6:c.*29C>A	ENSP00000466872.3:n.*29C>A
ENST00000354171.12:c.*3C>A	ENSP00000346103.7:n.*3C>A
ENST00000585480.1:c.297C>A	ENSP00000467900.1:p.Leu99=
ENST00000588919.5:c.538C>A	ENSP00000464989.3:p.Pro180Thr
ENST00000589115.5:c.*29C>A	ENSP00000466872.2:n.*29C>A
ENST00000592940.2:n.968C>A
ENST00000611653.4:c.*3C>A	ENSP00000483655.1:n.*3C>A
ENST00000616066.4:c.*3C>A	ENSP00000485000.1:n.*3C>A
ENST00000622390.4:c.*3C>A	ENSP00000477503.1:n.*3C>A
NM_001039847.2:c.619C>A	NP_001034936.1:p.Pro207Thr
NM_001039848.2:c.*3C>A	NP_001034937.1:n.*3C>A
NM_002085.4:c.*3C>A	NP_002076.2:n.*3C>A
NM_001039848.3:c.*3C>A	NP_001034937.1:n.*3C>A
NM_001039847.3:c.619C>A	NP_001034936.1:p.Pro207Thr
NM_001039848.4:c.*3C>A	NP_001034937.1:n.*3C>A
NM_001367832.1:c.*3C>A	NP_001354761.1:n.*3C>A
NM_002085.5:c.*3C>A MANE Select	NP_002076.2:n.*3C>A