Canonical Allele Identifier: CA9037124

Gene: GPX4

Linked Data

• ClinVar Variation Id: 2360311
• ClinVar RCV Id: RCV002986756
• dbSNP Id: rs772251077
• ExAC: 19:1104052 G / T
• gnomAD v2: 19-1104052-G-T
• gnomAD v3: 19-1104053-G-T
• gnomAD v4: 19-1104053-G-T
• MyVariant Identifiers: chr19:g.1104052G>T (hg19) ; chr19:g.1104053G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104053G>T , CM000681.2:g.1104053G>T	GRCh38
NC_000019.9:g.1104052G>T , CM000681.1:g.1104052G>T	GRCh37
NC_000019.8:g.1055052G>T	NCBI36
NG_050621.1:g.5128G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706713.1:c.10G>T	ENSP00000516510.1:p.Gly4Cys
ENST00000354171.13:c.10G>T MANE Select	ENSP00000346103.7:p.Gly4Cys
ENST00000589115.6:c.10G>T	ENSP00000466872.3:p.Gly4Cys
ENST00000354171.12:c.10G>T	ENSP00000346103.7:p.Gly4Cys
ENST00000589115.5:c.10G>T	ENSP00000466872.2:p.Gly4Cys
ENST00000611653.4:c.-72G>T	ENSP00000483655.1:n.-72G>T
ENST00000616066.4:c.10G>T	ENSP00000485000.1:p.Gly4Cys
NM_001039847.2:c.10G>T	NP_001034936.1:p.Gly4Cys
NM_002085.4:c.10G>T	NP_002076.2:p.Gly4Cys
NM_001039847.3:c.10G>T	NP_001034936.1:p.Gly4Cys
NM_002085.5:c.10G>T MANE Select	NP_002076.2:p.Gly4Cys