Canonical Allele Identifier: CA402937513

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105719G>A (hg19) ; chr19:g.1105720G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105720G>A , CM000681.2:g.1105720G>A	GRCh38
NC_000019.9:g.1105719G>A , CM000681.1:g.1105719G>A	GRCh37
NC_000019.8:g.1056719G>A	NCBI36
NG_050621.1:g.6795G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.498G>A	ENSP00000473614.3:p.Met166Ile
ENST00000593032.6:c.306G>A	ENSP00000465828.4:p.Met102Ile
ENST00000706713.1:c.381G>A	ENSP00000516510.1:p.Met127Ile
ENST00000706714.1:c.306G>A	ENSP00000516511.1:p.Met102Ile
ENST00000706715.1:c.3G>A	ENSP00000516512.1:p.Met1Ile
ENST00000354171.13:c.387G>A MANE Select	ENSP00000346103.7:p.Met129Ile
ENST00000589115.6:c.387G>A	ENSP00000466872.3:p.Met129Ile
ENST00000354171.12:c.387G>A	ENSP00000346103.7:p.Met129Ile
ENST00000585362.6:c.498G>A	ENSP00000473614.2:p.Met166Ile
ENST00000585480.1:c.120G>A	ENSP00000467900.1:p.Met40Ile
ENST00000587648.5:c.267G>A	ENSP00000468349.1:p.Met89Ile
ENST00000588919.5:c.306G>A	ENSP00000464989.3:p.Met102Ile
ENST00000589115.5:c.387G>A	ENSP00000466872.2:p.Met129Ile
ENST00000592940.2:n.326G>A
ENST00000593032.5:c.306G>A	ENSP00000465828.3:p.Met102Ile
ENST00000611653.4:c.306G>A	ENSP00000483655.1:p.Met102Ile
ENST00000616066.4:c.384G>A	ENSP00000485000.1:p.Met128Ile
ENST00000622390.4:c.495G>A	ENSP00000477503.1:p.Met165Ile
NM_001039847.2:c.387G>A	NP_001034936.1:p.Met129Ile
NM_001039848.2:c.498G>A	NP_001034937.1:p.Met166Ile
NM_002085.4:c.387G>A	NP_002076.2:p.Met129Ile
NM_001039848.3:c.498G>A	NP_001034937.1:p.Met166Ile
NM_001039847.3:c.387G>A	NP_001034936.1:p.Met129Ile
NM_001039848.4:c.498G>A	NP_001034937.1:p.Met166Ile
NM_001367832.1:c.306G>A	NP_001354761.1:p.Met102Ile
NM_002085.5:c.387G>A MANE Select	NP_002076.2:p.Met129Ile