Canonical Allele Identifier: CA783222413

Gene: GPX4

Linked Data

• dbSNP Id: rs970697715
• gnomAD v3: 19-1104034-C-G
• gnomAD v4: 19-1104034-C-G
• MyVariant Identifiers: chr19:g.1104033C>G (hg19) ; chr19:g.1104034C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104034C>G , CM000681.2:g.1104034C>G	GRCh38
NC_000019.9:g.1104033C>G , CM000681.1:g.1104033C>G	GRCh37
NC_000019.8:g.1055033C>G	NCBI36
NG_050621.1:g.5109C>G

Transcript Alleles

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