Canonical Allele Identifier: CA402934188

Gene: GPX4

Linked Data

• gnomAD v4: 19-1104072-T-G
• MyVariant Identifiers: chr19:g.1104071T>G (hg19) ; chr19:g.1104072T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104072T>G , CM000681.2:g.1104072T>G	GRCh38
NC_000019.9:g.1104071T>G , CM000681.1:g.1104071T>G	GRCh37
NC_000019.8:g.1055071T>G	NCBI36
NG_050621.1:g.5147T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593032.6:c.-53T>G	ENSP00000465828.4:n.-53T>G
ENST00000706713.1:c.29T>G	ENSP00000516510.1:p.Leu10Arg
ENST00000706714.1:c.-53T>G	ENSP00000516511.1:n.-53T>G
ENST00000354171.13:c.29T>G MANE Select	ENSP00000346103.7:p.Leu10Arg
ENST00000589115.6:c.29T>G	ENSP00000466872.3:p.Leu10Arg
ENST00000354171.12:c.29T>G	ENSP00000346103.7:p.Leu10Arg
ENST00000589115.5:c.29T>G	ENSP00000466872.2:p.Leu10Arg
ENST00000593032.5:c.-53T>G	ENSP00000465828.3:n.-53T>G
ENST00000611653.4:c.-53T>G	ENSP00000483655.1:n.-53T>G
ENST00000616066.4:c.29T>G	ENSP00000485000.1:p.Leu10Arg
NM_001039847.2:c.29T>G	NP_001034936.1:p.Leu10Arg
NM_002085.4:c.29T>G	NP_002076.2:p.Leu10Arg
NM_001039847.3:c.29T>G	NP_001034936.1:p.Leu10Arg
NM_001367832.1:c.-53T>G	NP_001354761.1:n.-53T>G
NM_002085.5:c.29T>G MANE Select	NP_002076.2:p.Leu10Arg