Canonical Allele Identifier: CA402934229

Gene: GPX4

Linked Data

• dbSNP Id: rs1356892049
• gnomAD v2: 19-1104094-G-A
• gnomAD v4: 19-1104095-G-A
• MyVariant Identifiers: chr19:g.1104094G>A (hg19) ; chr19:g.1104095G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104095G>A , CM000681.2:g.1104095G>A	GRCh38
NC_000019.9:g.1104094G>A , CM000681.1:g.1104094G>A	GRCh37
NC_000019.8:g.1055094G>A	NCBI36
NG_050621.1:g.5170G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000593032.6:c.-30G>A	ENSP00000465828.4:n.-30G>A
ENST00000706713.1:c.52G>A	ENSP00000516510.1:p.Ala18Thr
ENST00000706714.1:c.-30G>A	ENSP00000516511.1:n.-30G>A
ENST00000354171.13:c.52G>A MANE Select	ENSP00000346103.7:p.Ala18Thr
ENST00000589115.6:c.52G>A	ENSP00000466872.3:p.Ala18Thr
ENST00000354171.12:c.52G>A	ENSP00000346103.7:p.Ala18Thr
ENST00000588919.5:c.-30G>A	ENSP00000464989.3:n.-30G>A
ENST00000589115.5:c.52G>A	ENSP00000466872.2:p.Ala18Thr
ENST00000593032.5:c.-30G>A	ENSP00000465828.3:n.-30G>A
ENST00000611653.4:c.-30G>A	ENSP00000483655.1:n.-30G>A
ENST00000616066.4:c.52G>A	ENSP00000485000.1:p.Ala18Thr
NM_001039847.2:c.52G>A	NP_001034936.1:p.Ala18Thr
NM_002085.4:c.52G>A	NP_002076.2:p.Ala18Thr
NM_001039847.3:c.52G>A	NP_001034936.1:p.Ala18Thr
NM_001367832.1:c.-30G>A	NP_001354761.1:n.-30G>A
NM_002085.5:c.52G>A MANE Select	NP_002076.2:p.Ala18Thr