Canonical Allele Identifier: CA402934157

Gene: GPX4

Linked Data

• dbSNP Id: rs1379818943
• gnomAD v3: 19-1104054-G-T
• gnomAD v4: 19-1104054-G-T
• MyVariant Identifiers: chr19:g.1104053G>T (hg19) ; chr19:g.1104054G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104054G>T , CM000681.2:g.1104054G>T	GRCh38
NC_000019.9:g.1104053G>T , CM000681.1:g.1104053G>T	GRCh37
NC_000019.8:g.1055053G>T	NCBI36
NG_050621.1:g.5129G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706713.1:c.11G>T	ENSP00000516510.1:p.Gly4Val
ENST00000354171.13:c.11G>T MANE Select	ENSP00000346103.7:p.Gly4Val
ENST00000589115.6:c.11G>T	ENSP00000466872.3:p.Gly4Val
ENST00000354171.12:c.11G>T	ENSP00000346103.7:p.Gly4Val
ENST00000589115.5:c.11G>T	ENSP00000466872.2:p.Gly4Val
ENST00000611653.4:c.-71G>T	ENSP00000483655.1:n.-71G>T
ENST00000616066.4:c.11G>T	ENSP00000485000.1:p.Gly4Val
NM_001039847.2:c.11G>T	NP_001034936.1:p.Gly4Val
NM_002085.4:c.11G>T	NP_002076.2:p.Gly4Val
NM_001039847.3:c.11G>T	NP_001034936.1:p.Gly4Val
NM_002085.5:c.11G>T MANE Select	NP_002076.2:p.Gly4Val