Canonical Allele Identifier: CA631018522

Gene: GPX4

Linked Data

• dbSNP Id: rs1285528726
• gnomAD v2: 19-1103993-A-G
• gnomAD v3: 19-1103994-A-G
• gnomAD v4: 19-1103994-A-G
• MyVariant Identifiers: chr19:g.1103993A>G (hg19) ; chr19:g.1103994A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1103994A>G , CM000681.2:g.1103994A>G	GRCh38
NC_000019.9:g.1103993A>G , CM000681.1:g.1103993A>G	GRCh37
NC_000019.8:g.1054993A>G	NCBI36
NG_050621.1:g.5069A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706713.1:c.-50A>G	ENSP00000516510.1:n.-50A>G
ENST00000354171.13:c.-50A>G MANE Select	ENSP00000346103.7:n.-50A>G
ENST00000354171.12:c.-50A>G	ENSP00000346103.7:n.-50A>G
ENST00000616066.4:c.-50A>G	ENSP00000485000.1:n.-50A>G
NM_001039847.2:c.-50A>G	NP_001034936.1:n.-50A>G
NM_002085.4:c.-50A>G	NP_002076.2:n.-50A>G
NM_001039847.3:c.-50A>G	NP_001034936.1:n.-50A>G
NM_002085.5:c.-50A>G MANE Select	NP_002076.2:n.-50A>G